6,881 Quality Analyst jobs in the United States

Job Title: Quality Control AnalystJob Description
As a Quality Control Analyst, you will perform routine testing support and contribute to various projects. Your primary focus will be on qPCR testing with samples requiring a 7-hour turnaround time, necessitating a collaborative team effort. The testing involves in-process testing on raw materials, typically of pig origin, and finished product testing of pancreatin powder. You will be responsible for contaminant monitoring, environmental monitoring, and instrument calibration and maintenance while samples are running. Additionally, you will be trained on validation tasks, including validating centrifuges, spectrophotometers, and liquid handler robots, as well as software programming and method drafting.
Responsibilities
+ Perform routine qPCR testing with a 7-hour turnaround time.
+ Conduct in-process testing on raw materials and finished product testing.
+ Extract RNA from tissue samples.
+ Monitor contaminants and environmental conditions.
+ Calibrate and maintain laboratory instruments.
+ Prepare inventory and reagents.
+ Validate lab equipment and spaces.
+ Run speciation assays to identify and quantify species within samples.
Essential Skills
+ Proficiency in PCR and QC testing.
+ Understanding of method development and quality control.
+ Knowledge of GMP regulations.
+ Biology and pharmaceutical expertise.
+ Environmental monitoring skills.
+ Familiarity with FDA guidelines.
+ Molecular biology and microbiology experience.
+ Proficiency in laboratory assays.
Additional Skills & Qualifications
+ High School Diploma or G.E.D. required; bachelor's degree in Microbiology or related discipline preferred.
+ 2+ years of PCR/Micro Lab experience preferred for Associate QC Analyst.
+ 2+ years required with GMP for QC Analyst.
+ 5+ years required with GMP for Sr QC Analyst.
Work Environment
You will work in a brand new laboratory with a laid-back yet driven team culture that values hard work and dedication. The position requires working 2nd shift from 12 pm to 10 pm, Wednesday to Saturday, with a differential and incentive pay. Initial training will be conducted during the first week on the 1st shift, followed by a transition to your designated shift.
Pay and Benefits
The pay range for this position is $22.00 - $43.26/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Madison,WI.
Application Deadline
This position is anticipated to close on Jul 21, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Intro Marketing Language:

Join a team that supports your career growth, advancement and expanding opportunities! At JPMorgan Chase we take pride in valuing our employees' individualities, while supporting an inclusive culture of teamwork.

Job Summary:

As a Quality Control Analyst within Loan Accounting, you will be part of a team dedicated to navigating the dynamic landscape of client expectations and product complexities. Your role in Wholesale Lending Services is crucial in ensuring the delivery of top-tier products and services to our clients, maintaining the highest quality standards. You will be responsible for conducting quality reviews on the system of record for both new and existing credit facilities.

Job Responsibilities:

• Evaluate, identify, and report any inconsistences between the supporting documentation relative to the proposal data entered in accordance with internal risk policies
• Ensure organizational requests, queries, and issues sent to the team are actioned accurately and timely
• Adhere to production queues, exception reporting, and Key Performance Indicators
• Collaborate with Operations, Credit, and Controls in resolving items and preparing weekly ad hoc reports when requested

Required Qualifications, Capabilities, and Skills:

• Experience reading and interpreting loan documentation and/or working with credit products such as revolving lines of credit, term loans, commercial cards, letters of credit
• Demonstrated decision-making skills
• Strong oral and written communication skills
• Analytical mindset with the ability to probe sensitive issues while maintaining the highest level of integrity and objectivity
• Ability to prioritize tasks and pivot in response to new developments

Preferred Qualifications, Capabilities, and Skills:

• Bachelor's Degree
• Intermediate use of Microsoft Word, Excel, Access
• Experience with loan accounting systems, such as LoanIQ

JPMorganChase, one of the oldest financial institutions, offers innovative financial solutions to millions of consumers, small businesses and many of the world's most prominent corporate, institutional and government clients under the J.P. Morgan and Chase brands. Our history spans over 200 years and today we are a leader in investment banking, consumer and small business banking, commercial banking, financial transaction processing and asset management.

We offer a competitive total rewards package including base salary determined based on the role, experience, skill set and location. Those in eligible roles may receive commission-based pay and/or discretionary incentive compensation, paid in the form of cash and/or forfeitable equity, awarded in recognition of individual achievements and contributions. We also offer a range of benefits and programs to meet employee needs, based on eligibility. These benefits include comprehensive health care coverage, on-site health and wellness centers, a retirement savings plan, backup childcare, tuition reimbursement, mental health support, financial coaching and more. Additional details about total compensation and benefits will be provided during the hiring process.

We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. We do not discriminate on the basis of any protected attribute, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. We also make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as mental health or physical disability needs. Visit our FAQs for more information about requesting an accommodation.

JPMorgan Chase & Co. is an Equal Opportunity Employer, including Disability/Veterans

Base Pay/Salary
Chicago,IL $59,470.00 - $85,300.00

Quality Control Analyst III in Camarillo, CA
Build your future at Curia, where our work has the power to save lives.
Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.
We proudly offer
+ Generous benefit options (eligible first day of employment)
+ Paid training, vacation and holidays (vacation accrual begins on first day of employment)
+ Career advancement opportunities
+ Education reimbursement
+ 401K program with matching contributions
+ Learning platform
+ And more!
Summary
The Quality Control Analyst III is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw materials, in-process, end product, and stability samples.
Essential job duties
+ Perform complex testing and data evaluation
+ Perform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues
+ Participate in or assist with test method validations
+ Evaluate data for trends
+ Support supervisors in OOS Investigations and complete CAPA requirements
+ Interact with outside departments including attending meetings, providing updates, etc.
+ Coordinate testing performed at outside testing labs, raw materials, etc.
+ Maintain a detailed and accurate recording of activities and results on paperwork
+ Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools
+ Train upon and understand methods, equipment and standard operating procedures
+ Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures
+ Support equipment upkeep
+ Prepare and order supplies, as necessary
+ Enter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management
+ Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry
+ Interact with other departments within the company for testing needs and scheduling
+ May lead departmental projects with the opportunity to participate in or lead cross-functional teams, including continuous improvement projects and new customer teams
+ May lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results.
Education, experience, certification and licensures
Required
+ Bachelor's degree in Chemistry or related field
+ Minimum 5-7 year's pharmaceutical experience or equivalent combination of education and experience
Preferred
+ Experience working in cGMP or GLP pharmaceutical industry environment
Knowledge, skills and abilities
+ Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public
+ Ability to meet deadlines and work under pressure with limited supervision
+ Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently
+ Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations
+ Ability to write reports, business correspondence, and procedure manuals
+ Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations
+ Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis
+ Ability to define problems, collect data, establish facts, and draw valid conclusions
+ Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables
+ Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems
+ Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus
Pay Range
$81,000 - $100,924
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
#LI-MM2

QUALITY CONTROL ANALYST II in Camarillo, CA
Build your future at Curia, where our work has the power to save lives
Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.
We proudly offer
+ Generous benefit options (eligible first day of employment)
+ Paid training, vacation and holidays (vacation accrual begins on first day of employment)
+ Career advancement opportunities
+ Education reimbursement
+ 401K program with matching contributions
+ Learning platform
+ And more!
The Quality Control Analyst II is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications.
Essential job duties
+ Perform analytical testing for incoming, in-process and final products, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, Total Organic Carbon analyzer, etc.
+ Perform chromatography (HPLC/UPLC, GC) with minimal qualification and training, wet chemistry assays, analytical chemistry assays, Capillary Electrophoresis, ELISA, HPLC/UPLC, GC, IR, UV, etc. and raw material testing and/or sampling
+ Back up for QC analytical instrument maintenance and calibration
+ Perform QC general laboratory equipment maintenance, laboratory housekeeping, hazardous waste handling, and preparation of the laboratory for audits
+ Perform or assist with QC method qualifications, transfers, and validations
+ Perform QC method development
+ Perform cleaning validation studies
+ Assist with the evaluation of new equipment and processes
+ Assist in the review of QC data and provide summaries to management as needed
+ Assist QC Management, as needed, in the completion of OOS, deviations, and CAPAs investigations for QC
+ Backup for QC analytical sample receipt for internal testing, outside laboratory testing, login, processing, shipment, tracking, distribution of test results, and closure
Education, experience, certification and licensures Required
+ Bachelor's degree in Chemistry or related field
+ Minimum 3-5 years' experience in pharmaceutical industry environment or equivalent combination of education and experience
Preferred
+ Experience working in cGMP or GLP pharmaceutical industry environment
Knowledge, skills and abilities
+ Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public
+ Ability to meet deadlines and work under pressure with limited supervision
+ Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently
+ Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations
+ Ability to write reports, business correspondence, and procedure manuals
+ Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations
+ Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis
+ Ability to define problems, collect data, establish facts, and draw valid conclusions
+ Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables
+ Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems
+ Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus
Salary: $70,000 - $86,900/year.
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
#LI-MM2

**Description**
**BANC OF CALIFORNIA AND YOUR CAREER**
Banc of California, Inc. (NYSE: BANC) is a bank holding company headquartered in Los Angeles with one wholly-owned banking subsidiary, Banc of California (the "bank"). Banc of California is one of the nation's premier relationship-based business banks focused on providing banking and treasury management services to small, middle-market, and venture-backed businesses. Banc of California offers a broad range of loan and deposit products and services, with full-service branches throughout California and Denver, Colorado, as well as full-stack payment processing solutions through its subsidiary, Deepstack Technologies. The bank is committed to its local communities by supporting organizations that provide financial literacy and job training, small business support, affordable housing, and more.
At Banc of California, our success is driven by our people, and we take pride in fostering an environment where everyone can reach their full potential. We embrace a culture of empowerment, progressive thinking, and entrepreneurial spirit, ensuring our team members have an opportunity to make an impact and play an important role in the future of Banc of California. Our core values - Entrepreneurialism, Operational Excellence, and Superior Analytics - empower us in creating a dynamic and inclusive workplace. We are committed to supporting your growth and well-being with comprehensive benefits, career development programs, a variety of employee resource groups, and more. TOGETHER WE WIN®
**THE OPPORTUNITY**
The BSA Quality Control Analyst will assist in department efforts to adhere to the legal and regulatory environment as it relates to the Bank Secrecy Act and Anti-Money Laundering. The analyst will conduct ongoing analysis and quality control testing on various BSA/AML tasks including, but not limited to: quality and accuracy reviews of Suspicious Activity Reporting, AML alert case decisions and documentation, AML case quality, documentation and disposition of the case, Currency Transaction Reporting accuracy, OFAC Compliance, Customer Due Diligence and Enhanced Due Diligence quality, documentation and accuracy, Fraud Compliance, as well as various additional BSA/AML related tasks. Analysis will be reviewing completed work to ensure it meets governmental regulations, accuracy and quality standards, identify new and existing patterns and trends, and completing regular reports that will be presented to BSA/AML Management. Performs all duties in accordance with the Company's policies and procedures, all U.S. state and federal laws and regulations, wherein the Company operates.
**HOW YOU'LL MAKE A DIFFERENCE**
+ Performs quality control testing employing various methods such as data analysis, observation, interviews, or other investigative techniques.
+ Conduct customer and transaction testing and report writing as assigned.
+ Partners with business unit and/or individuals as necessary in conducting quality control testing related to BSA/AML and OFAC compliance.
+ Review and filing of Suspicious Activity Reports with FinCEN
+ Identifies potential BSA/AML & OFAC risk and escalates issues to management.
+ Recommends and follows up on corrective action.
+ Assist BSA/AML QC Manager with developing QC reporting and metrics.
+ Assist BSA/AML QC Manager with maintaining QC Policies and Procedures.
+ Treat people with respect; keep commitments; inspire the trust of others; work ethically and with integrity; uphold organizational values; accept responsibility for own actions.
+ Demonstrates knowledge of and adherence to EEO policy; shows respect and sensitivity for cultural differences; educates others on the value of diversity; promotes working environment free of harassment of any type; builds a diverse workforce and supports affirmative action.
+ Follows policies and procedures; completes tasks correctly and on time; supports the company's goals and values.
+ Performs the position safely, without endangering the health or safety to themselves or others and will be expected to report potentially unsafe conditions. The employee shall comply with occupational safety and health standards and all rules, regulations and orders issued pursuant to the OSHA Act of 1970, which are applicable to one's own actions and conduct.
+ Performs other duties and projects as assigned.
**WHAT YOU'LL BRING**
+ Experience:
+ Required: 2+ years of Bank Secrecy Act and Anti-Money Laundering work experience
+ Preferred: Experience with Enhanced Due Diligence procedures and methodology
+ Education & Certifications:
+ Required:
+ High School Diploma or equivalent
+ Preferred:
+ College Diploma
+ CAMS certification
+ Skills, Behaviors, & Knowledge
+ Required:
+ Subject Matter Expert of banking regulations (specifically BSA/AML and OFAC)
+ Strong Investigative, Analytical and problem solving skills; ability to use logic, reason and sound judgment
+ Ability to work both independently and with team members, under tight deadlines
+ Strong interpersonal skills and ability to communicate effectively both verbally and in writing
+ Ability to handle highly confidential information professionally and with appropriate discretion
+ Proficiency in Microsoft Office including Excel
+ The ability to read, write and communicate well in English
+ Preferred:
+ Familiarity of SAR filing systems
**HOW WE'LL SUPPORT YOU**
+ **Financial Security:** You will be eligible to participate in the company's 401k plan which includes a company match and immediate vesting.
+ **Health & Well-Being:** We offer comprehensive insurance options including medical, dental, vision, AD&D, supplemental life, long-term disability, pre-tax Health Savings Account with employer contributions, and pre-tax Flexible Spending Account (FSA).
+ **Building & Supporting Your Family:** Banc of California partners with providers that offeradoption, surrogacy, and fertility assistance as well as paid parental leave and family support solutions including care options for your family.
+ **Paid Time Away:** Eligible team members receive paid vacation days, holidays, and volunteer time off.
+ **Career Growth Opportunities:** To support career growth of our team members, we offer tuition reimbursement, an annual mentorship program, leadership development resources, access to LinkedIn Learning, and more.
**SALARY RANGE**
The full-time base salary range for this position is $68,640 - $81,000 a year. The base salary ultimately offered is determined through a review of education, industry experience, training, knowledge, skills, abilities of the applicant in alignment with market data and other factors.
Banc of California is an equal opportunity employer committed to creating a diverse workforce. All qualified applicants will receive consideration for employment without regard to age (40 and over), ancestry, color, religious creed (including religious dress and grooming practices), denial of Family and Medical Care Leave, disability (mental and physical) including HIV and AIDS, marital status, medical condition (cancer and genetic characteristics), genetic information, military and veteran status, national origin (including language use restrictions), race, sex (which includes pregnancy, childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), gender, gender identity, gender expression, and sexual orientation. If you require reasonable accommodation as part of the application process, please contact Talent Acquisition.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights ( notice from the Department of Labor.
Equal Opportunity Employer
PacWest Bancorp and its affiliates are fully committed to the principles of equal opportunity and diversity. We take pride in building a workplace culture where all employees feel supported and respected, and have equal access to career and development opportunities without regard to race, religion/creed, color, national origin, age, marital status, ancestry, sex, gender (including pregnancy, childbirth, breastfeeding or related medical conditions), gender identity/expression, sexual orientation, veteran status, physical or mental disability, medical condition, military status, genetic information, or any other characteristic protected by federal, state or local laws.

**Description**
**BANC OF CALIFORNIA AND YOUR CAREER**
Banc of California, Inc. (NYSE: BANC) is a bank holding company headquartered in Los Angeles with one wholly-owned banking subsidiary, Banc of California (the "bank"). Banc of California is one of the nation's premier relationship-based business banks focused on providing banking and treasury management services to small, middle-market, and venture-backed businesses. Banc of California offers a broad range of loan and deposit products and services, with full-service branches throughout California and Denver, Colorado, as well as full-stack payment processing solutions through its subsidiary, Deepstack Technologies. The bank is committed to its local communities by supporting organizations that provide financial literacy and job training, small business support, affordable housing, and more.
At Banc of California, our success is driven by our people, and we take pride in fostering an environment where everyone can reach their full potential. We embrace a culture of empowerment, progressive thinking, and entrepreneurial spirit, ensuring our team members have an opportunity to make an impact and play an important role in the future of Banc of California. Our core values - Entrepreneurialism, Operational Excellence, and Superior Analytics - empower us in creating a dynamic and inclusive workplace. We are committed to supporting your growth and well-being with comprehensive benefits, career development programs, a variety of employee resource groups, and more. TOGETHER WE WIN®
**THE OPPORTUNITY**
The BSA Quality Control Analyst will assist in department efforts to adhere to the legal and regulatory environment as it relates to the Bank Secrecy Act and Anti-Money Laundering. The analyst will conduct ongoing analysis and quality control testing on various BSA/AML tasks including, but not limited to: quality and accuracy reviews of Suspicious Activity Reporting, AML alert case decisions and documentation, AML case quality, documentation and disposition of the case, Currency Transaction Reporting accuracy, OFAC Compliance, Customer Due Diligence and Enhanced Due Diligence quality, documentation and accuracy, Fraud Compliance, as well as various additional BSA/AML related tasks. Analysis will be reviewing completed work to ensure it meets governmental regulations, accuracy and quality standards, identify new and existing patterns and trends, and completing regular reports that will be presented to BSA/AML Management. Performs all duties in accordance with the Company's policies and procedures, all U.S. state and federal laws and regulations, wherein the Company operates.
**HOW YOU'LL MAKE A DIFFERENCE**
+ Performs quality control testing employing various methods such as data analysis, observation, interviews, or other investigative techniques.
+ Conduct customer and transaction testing and report writing as assigned.
+ Partners with business unit and/or individuals as necessary in conducting quality control testing related to BSA/AML and OFAC compliance.
+ Review and filing of Suspicious Activity Reports with FinCEN
+ Identifies potential BSA/AML & OFAC risk and escalates issues to management.
+ Recommends and follows up on corrective action.
+ Assist BSA/AML QC Manager with developing QC reporting and metrics.
+ Assist BSA/AML QC Manager with maintaining QC Policies and Procedures.
+ Treat people with respect; keep commitments; inspire the trust of others; work ethically and with integrity; uphold organizational values; accept responsibility for own actions.
+ Demonstrates knowledge of and adherence to EEO policy; shows respect and sensitivity for cultural differences; educates others on the value of diversity; promotes working environment free of harassment of any type; builds a diverse workforce and supports affirmative action.
+ Follows policies and procedures; completes tasks correctly and on time; supports the company's goals and values.
+ Performs the position safely, without endangering the health or safety to themselves or others and will be expected to report potentially unsafe conditions. The employee shall comply with occupational safety and health standards and all rules, regulations and orders issued pursuant to the OSHA Act of 1970, which are applicable to one's own actions and conduct.
+ Performs other duties and projects as assigned.
**WHAT YOU'LL BRING**
+ Experience:
+ Required: 2+ years of Bank Secrecy Act and Anti-Money Laundering work experience
+ Preferred: Experience with Enhanced Due Diligence procedures and methodology
+ Education & Certifications:
+ Required:
+ High School Diploma or equivalent
+ Preferred:
+ College Diploma
+ CAMS certification
+ Skills, Behaviors, & Knowledge
+ Required:
+ Subject Matter Expert of banking regulations (specifically BSA/AML and OFAC)
+ Strong Investigative, Analytical and problem solving skills; ability to use logic, reason and sound judgment
+ Ability to work both independently and with team members, under tight deadlines
+ Strong interpersonal skills and ability to communicate effectively both verbally and in writing
+ Ability to handle highly confidential information professionally and with appropriate discretion
+ Proficiency in Microsoft Office including Excel
+ The ability to read, write and communicate well in English
+ Preferred:
+ Familiarity of SAR filing systems
**HOW WE'LL SUPPORT YOU**
+ **Financial Security:** You will be eligible to participate in the company's 401k plan which includes a company match and immediate vesting.
+ **Health & Well-Being:** We offer comprehensive insurance options including medical, dental, vision, AD&D, supplemental life, long-term disability, pre-tax Health Savings Account with employer contributions, and pre-tax Flexible Spending Account (FSA).
+ **Building & Supporting Your Family:** Banc of California partners with providers that offeradoption, surrogacy, and fertility assistance as well as paid parental leave and family support solutions including care options for your family.
+ **Paid Time Away:** Eligible team members receive paid vacation days, holidays, and volunteer time off.
+ **Career Growth Opportunities:** To support career growth of our team members, we offer tuition reimbursement, an annual mentorship program, leadership development resources, access to LinkedIn Learning, and more.
**SALARY RANGE**
The full-time base salary range for this position is $68,640 - $81,000 a year. The base salary ultimately offered is determined through a review of education, industry experience, training, knowledge, skills, abilities of the applicant in alignment with market data and other factors.
Banc of California is an equal opportunity employer committed to creating a diverse workforce. All qualified applicants will receive consideration for employment without regard to age (40 and over), ancestry, color, religious creed (including religious dress and grooming practices), denial of Family and Medical Care Leave, disability (mental and physical) including HIV and AIDS, marital status, medical condition (cancer and genetic characteristics), genetic information, military and veteran status, national origin (including language use restrictions), race, sex (which includes pregnancy, childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), gender, gender identity, gender expression, and sexual orientation. If you require reasonable accommodation as part of the application process, please contact Talent Acquisition.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights ( notice from the Department of Labor.
Equal Opportunity Employer
PacWest Bancorp and its affiliates are fully committed to the principles of equal opportunity and diversity. We take pride in building a workplace culture where all employees feel supported and respected, and have equal access to career and development opportunities without regard to race, religion/creed, color, national origin, age, marital status, ancestry, sex, gender (including pregnancy, childbirth, breastfeeding or related medical conditions), gender identity/expression, sexual orientation, veteran status, physical or mental disability, medical condition, military status, genetic information, or any other characteristic protected by federal, state or local laws.

**Quality Control Analyst IV - Tech Transfer Team**
**Position Summary:**
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
The Boston-area facility is Catalent's global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America.
Catalent Pharma Solutions is hiring a Quality Control (QC) Analyst IV who is a key analytical leader in a cGMP (Good Manufacturing Practices) laboratory capable of both clinical development and commercial testing. This analyst is both a mentor and trainer to team members and serves as a backup to QC management.
**This is a full-time on-site salaried position: Monday - Friday 8:00AM - 4:30PM.**
**Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.**
**The Role:**
+ Operates analytical instrumentation (i.e. HPLC, UPLC, GC, UV-vis, FTIR, laser diffraction, Karl Fischer, etc.) for GMP testing of materials and product, for method transfers/validation, and for investigational purposes in a compliant and efficient manner
+ Performs data review and reporting (Certificate of Analysis (COA), reports, etc.). Statistically and critically analyzes data for trending and reporting in quarterly quality reviews and annual product reviews
+ Leads investigations for Deviations, Out Of Spec/Trend (OOS/OOT) results, and Product Quality Complaints
+ Monitors equipment and instrumentation to ensure efficient laboratory operations
+ Authors/Reviews/Approves controlled documents such as Standard Operating Procedures (SOPs), analytical test procedures, protocols, logbooks and checklists
+ Identifies and escalates both issues and opportunities for efficiencies on instruments and/or test executions; makes initial recommendations for possible solutions and/or corrective actions and implements solutions as appropriate
+ Trains and mentors team members on analytical instrumentation and material/product test methods. Leads team standup meetings and assists in laboratory scheduling
+ All other duties as assigned
**The Candidate:**
+ Bachelor's Degree in Physical or Chemical Sciences (life sciences) required
+ Minimum of eight (8) years of experience in a cGMP regulated environment required
+ Experience in MDI/DPI analytical test methods (i.e. Andersen Cascade Impactor and Emitted Dose techniques) preferred
+ Extensive experience with executing GMP QC test methods, generating associated data packages, auditing data packages generated by others, troubleshooting instrumentation, trending data and statistical analyses required
+ Demonstrated ability to lead and/or author investigations to determine root causes of OOTs and/or OOSs according to cGMP standards required
+ Ability to troubleshoot and repair analytical instrumentation such as HPLCs and UPLCs preferred
+ Chromatography skills using Empower and/or ChemStation required
+ Critical understanding of the importance of documentation and data traceability required
+ Physical requirements: Individual may be required to sit, stand, walk regularly and occasionally lift 0-50 pounds
**Why you should join Catalent:**
+ Defined career path and annual performance review and feedback process
+ Diverse, inclusive culture
+ Positive working environment focusing on continually improving processes to remain innovative
+ Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
+ 152 Hours + 8 paid holidays
+ Several Employee Resource Groups focusing on D&I
+ Dynamic, fast-paced work environment
+ Community engagement and green initiatives
+ Generous 401K match
+ Company match on donations to organizations
+ Medical, dental and vision benefits effective day one of employment
+ Tuition Reimbursement - Let us help you finish your degree or start a new degree!
+ WellHub program to promote overall physical wellness
+ Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories
**Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers ( to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE ( .

**Quality Control Analyst I**
**Position Summary:**
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
The Boston-area facility is Catalent's global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America.
Catalent Pharma Solutions in Chelsea is hiring a Quality Control (QC) Analyst I. Quality Control Analyst is responsible for executing QC testing and related microbial and analytical activities supporting product development, release and stability. These individual conducts routine and non-routine microbial, chemical and physical analyses of environmental/utilities monitoring samples, raw materials, in-process materials and drug products according to standard operating procedures. The Quality Control Analyst compiles data for documentation of test procedures that may include stability program testing and formulation studies, participates in the preparation of investigations, summaries and reports, and reviews data obtained for compliance to specifications. The Quality Control Analyst revises and updates standard operating procedures (SOPs) as needed.
**This is a full-time hourly role. This is on-site and the core hours are Monday - Friday 8:00AM-4:30PM .**
**Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.**
**The Role:**
+ Environmental Monitoring (EM) of classified cleanrooms, including total particulate, viable air and viable surface testing of ISO 8 cleanrooms
+ Performs analytical testing of spray dried powder using relevant methodologies (i.e. Delivered Dose, Anderson Cascade Impaction, Next Generation Impaction)
+ Performs a variety of microbiologic assays such as bioburden, sterility testing, growth promotion testing and microorganism isolation
+ Operates analytical instrumentation (i.e. Total Organic Carbon (TOC), Fourier Transform Infrared Spectroscopy (FTIR), laser diffraction, Karl Fischer); Critically analyzes data for reporting against specifications and/or protocols; Supports Laboratory and/or Quality Investigations
+ Monitors equipment and instrumentation used on a daily basis to ensure proper operation and calibration; Prepares solutions and diluents required for analytical testing. Monitor lab supply inventory
+ Participates in the construction and/or revision of SOP. Assists in the writing and updating of analytical test procedures, protocol, log books and checklists
+ Responsible for identifying and alerting a supervisor of issues on instruments and/or test executions; makes initial recommendations for possible solutions and/or corrective actions
+ All other duties as assigned
**The Candidate:**
+ Bachelor's Degree in Physical or Chemical Sciences (life sciences) required. No experience is required in a cGMP regulated environment, although it is highly preferred
+ Experience with executing QC test methods, generating associated data packages, auditing data packages generated by others, troubleshooting instrumentation, trending data and statistical analyses preferred
+ Familiarity with executing Standard Operating Procedures in a GMP setting preferred
+ Critical understanding of the importance of documentation and data traceability preferred
+ Working knowledge of cGMP's and their application to Quality Control preferred
+ Ability to effectively manage time and prioritize tasks independently to meet tight timelines and shifting priorities. Excellent oral and written communication skills
+ Physical requirements: Individual may be required to sit, stand, walk, and reach regularly and occasionally lift up to 50 pounds
**Why you should join Catalent:**
+ Defined career path and annual performance review and feedback process
+ Diverse, inclusive culture
+ Positive working environment focusing on continually improving processes to remain innovative
+ Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
+ 152 Hours + 8 paid holidays
+ Several Employee Resource Groups focusing on D&I
+ Dynamic, fast-paced work environment
+ Community engagement and green initiatives
+ Generous 401K match
+ Company match on donations to organizations
+ Medical, dental and vision benefits effective day one of employment
+ Tuition Reimbursement - Let us help you finish your degree or start a new degree!
+ WellHub program to promote overall physical wellness
+ Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories
**Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers ( to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE ( .