5,446 Manufacturing Qa jobs in the United States

**The Position**
Hillsboro Technical Operations (HTO) is a drug product & finished goods manufacturing organization responsible for the reliable delivery of Roche's commercial portfolio & pipeline products. The Operations organization at HTO is divided into 2 production streams, which combine to produce millions of units of life-saving medicine every year to patients around the world.
**The Opportunity:**
In this exciting role, you will provide direct manufacturing quality oversight at HTO. As part of a dynamic and inclusive team, you will partner with manufacturing and other stakeholders at the site and in the network to supply patients. You will apply knowledge of aseptic drug product manufacturing processes, of health authority expectations and industry standards. You will act as a mentor and coach for the organization.
+ You will act as key quality contact to manufacturing for discrepancy management, line support and batch review for commercial and launch products.
+ You will provide quality oversight related to operational activities, procedures and processes. You will ensure that investigations are accurate, include appropriate corrective actions, and follow regulations, industry guidelines and company standards.
+ You will apply your in-depth practical and conceptual knowledge in the manufacturing and quality functional areas at the site and within the company network.
+ You will support internal cGMP audits and Health Authority inspections as a technical resource and quality subject matter expert.
+ You will develop new approaches to complex problems. You will lead coordination and issue resolution across HTO Manufacturing Operations, support groups and/or projects (e.g. Operations Teams) as needed.
+ You will be responsible for setting the strategic direction and framework of one or multiple programs within HTO Quality in the areas of process development, process improvement, quality and compliance. You will own the deliverables within the established programs and lead teams in their execution in line with the site strategy.
+ You will be accountable for managing key operational support activities related to product transfers and new equipment/process start-up (manufacturing readiness and process design, documents, engineering runs, equipment set up, etc.).
**Who you are:**
+ You hold a Bachelor's degree (preferably within the Life Sciences or Engineering)
+ For a QA Specialist, you have at least 5 years of experience in the pharmaceutical industry. For a Senior QA Specialist, you have at least 8 years of experience in the pharmaceutical industry.
+ You are a strong problem-solver and have the demonstrated ability to troubleshoot and resolve process-related issues, ensuring efficient operations and regulatory compliance.
+ You possess a deep understanding of safety, quality systems, and quality assurance concepts including the application of current Good Manufacturing Practices (cGMPs) in aseptic processing and production.
+ You have a solid understanding of aseptic processing principles, regulations, and industry guidelines relevant to biologics processing, including knowledge of quality assurance principles, quality systems, microbiology, and sterility assurance.
+ Your interactions exhibit tactful and effective communication skills as they often involve complex and sensitive information.
+ You are able to gown into production space.
Preferred:
+ You have a Master's degree (preferably within the Life Sciences or Engineering)
+ You have experience in nPFS (nested pre-filled syringe) filling
+ You have experience in medical devices
The expected salary range for this position based on the primary location for this position of Hillsboro, OR is $75,000 - $39,400 for the QA Specialist level and 91,100 - 169,100 for the Senior QA Specialist. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Link to Benefits ( position is eligible for relocation benefits. It is not eligible for full time remote work arrangements.
#gnehtoquality
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants ( .

Job Description

Job Description

Sulzer is a leading engineering company with a proud heritage of innovation. Join our global team to grow your expertise and develop innovative solutions that enable a prosperous and more sustainable society.

We are looking for a/an Manufacturing Coordinator, QA & Logistics Specialist to join our Process Plants team in Cumming, GA.

Your main tasks and responsibilities:

• Define quality control procedures for fabricated components, mechanical/electrical assemblies, and field-installed systems to meet client, industry, and regulatory standards.
• Coordinate inspections of incoming parts, in-process fabrication, and finished goods prior to shipment.
• Identify and document non-conformities, lead root cause analysis efforts, and implement corrective/preventive actions.
• Support engineering and project management teams with documentation and certification needs including materials traceability, and QA/QC reporting packages.
• Manage the end-to-end logistics of transporting wastewater treatment equipment, system components, and field tools to customer sites and fabrication partners.
• Develop and optimize shipping plans, including carrier selection and route planning for large and complex systems requiring special handling.

To succeed in this role, you will need:

• 3+ years of experience in quality assurance, logistics, or manufacturing operations
• Knowledge of ISO standards, GMP, and other regulatory framework
• Solid understanding of quality control systems, logistics planning, and transportation management
• Strong analytical, problem-solving, and communication skills
• Excellent verbal and written communication skills, with ability to work collaboratively across teams

What we offer you:

• An innovative, vibrant, and agile culture
• Opportunities to develop as a professional and grow in areas of your interest from a world-class, progressive international company
• A competitive salary and robust company bonus plan
• 12 paid holidays plus additional PTO and company paid time off to volunteer
• Comprehensive benefits program
• Retirement plan matching with additional match benefits available after 1 year

No visa or work permit support can be provided for this role

Sulzer is an equal opportunity employer. We believe in the strength of a diverse workforce and are committed to offering an inclusive work environment.

We are proud to be recognized as a Top Employer 2025 in Brazil, China, Finland, Germany, Ireland, Switzerland, South Africa, the UK and the USA.

**Job Description:**
+ **Shift Hours: 6-4:30 PM PST+ OT as needed.**
+ Responsible for the final quality audit before shipment of systems, upgrades, and miscellaneous ship kits.
+ Collaborate closely with Manufacturing, Manufacturing Engineering, Master Scheduling, Production Control, Material handlers, Dock personnel and Packing contractors to ensure audits and quality inspections are completed so that products ship on time.
+ Demonstrate proficiency with SAP SW as well as the MS Office suite.
+ Clear communication and strong collaborative skills
+ Persevere against challenging and time constrained issues.
+ Inventing creative solutions to problems to ensure the job gets done on time.
+ Provide constructive process improvement recommendations.
+ Redline procedures as appropriate.
+ Assist in the training and development of new hires.
+ Support other product lines in plant clearance activities when necessary.
**Responsibilities:**
+ Auditing material against BOMs.
+ Evaluating the quality of packaging.
+ Visual spot check of part quality.
+ Ensure proper labelling of parts.
+ Consolidating piece parts into the correct shipping bin.
+ Working with Production Control and/or Manufacturing Engineering to resolve issues.
+ Coordinate material movement out of clean room.
+ Creating and maintaining Plant Clearance audit records.
**Experience:**
+ Quality Control exp. for Packaging & Production audits for semiconductor or manufacturing clients
**Skills:**
+ Auditing material against BOMs
+ Quality Control
+ SAP SW
+ MS Office suite
**Education:**
+ HS or equivalent practical experience.
**About US Tech Solutions:**
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit .
US Tech Solutions 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, disability, or status as a protected veteran.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
**Position Description:**
The Technician - QA - Manufacturing Logistics provides support to Regional Third-Party Logistics and Warehousing, based out of Brownsburg, IN. The QA Technician will support activities within Warehouse operations, including goods receipt, sampling, and outbound shipping process as well as perform incoming inspections of materials and sampling of items (components, printed packaging materials, etc.) utilizing SAP and LIMS. Persons must be able to lift items up to 50 pounds. The QA Technician's position is essential for maintaining quality systems and ensuring GMP compliance.
**Key Objectives/Deliverables:**
+ Provide direct quality oversight of third-party operations.
+ Author, documents including, but not limited to, procedures, change control proposals, deviations, and equipment qualifications.
+ Ensures all areas of oversight remain in quality compliance per SOPs and cGMP requirements.
+ Provide quality guidance and recommendations regarding materials, utilities, and maintenance.
+ Practices safety behaviors with proper PPE and lifting techniques. Supports all HSE Corporate and Site Goals.
+ Participate in aberrant data investigations.
+ Work with Lilly support groups and external partners to resolve or provide advice on receiving or shipping issues.
+ Evaluating damaged materials found on inbound shipments or within the warehouse and determine acceptability.
+ Evaluating temperature excursions on shipments received at the warehouse.
+ Identifies and assists in resolving issues on shipments (i.e. Incorrect quantity or product, contamination, etc.).
+ Performs appropriate transactions in SAP to ensure system represents appropriate status of material (QI, blocked, Investigate customer complaints.)
+ Work closely with site customers to report and resolve issues and improve the process.
+ Participate in and/or support recalls, as appropriate.
+ Conduct gap assessments of global requirements and ensure implementation of the governing standards.
+ Participate/lead self-inspection activities and support regulatory inspections/audits.
+ Maintain and improve quality systems.
**Basic Requirements:**
+ Must be able to lift up to 50 lbs.
+ Position is 8 hour days - Monday through Friday
+ Ability to work overtime, as required.
**Additional Preferences:**
+ Demonstrated strong written and verbal communications skills.
+ Strong attention to detail.
+ Proficiency with computer system applications.
+ Knowledge of cGMPs and quality systems.
+ Excellent interpersonal skills and networking skills.
+ Ability to organize and prioritize multiple tasks.
+ Previous experience in QA, QC, Manufacturing, Engineering, Tech Services or Regulatory Affairs.
+ Experience in inventory management systems (EWM, SAP, etc.)
**Education Requirements:**
+ High school diploma or two-year degree
**Other Information:**
+ Must complete Learning Plan for job responsibilities
+ No certifications required.
+ Tasks may require executing activities which require wearing appropriate PPE.
+ Manufacturing is a 24 hour/day operation, off-hour and weekend support may be required.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$28.12 - $45.48
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly

Our client, a leader in the advanced manufacturing sector, is seeking a highly experienced Senior Manufacturing Quality Control Specialist to join their dynamic team in San Francisco, California, US . This role will be pivotal in ensuring the highest standards of quality across all production processes. The ideal candidate will possess a deep understanding of quality management systems, statistical process control (SPC), and various inspection methodologies. You will be responsible for developing, implementing, and maintaining quality assurance procedures to meet and exceed industry regulations and customer expectations.

Responsibilities:

• Develop and implement comprehensive quality control plans and procedures for manufacturing processes.
• Conduct regular inspections and audits of production lines to ensure compliance with quality standards.
• Analyze production data using statistical methods to identify trends, root causes of defects, and areas for improvement.
• Oversee the calibration and maintenance of quality control equipment.
• Investigate product non-conformances and implement corrective and preventive actions (CAPA).
• Train and mentor junior quality control technicians and manufacturing personnel on quality standards and procedures.
• Collaborate with engineering, production, and R&D teams to resolve quality issues and improve product design.
• Prepare detailed quality reports for management, highlighting key performance indicators and improvement initiatives.
• Ensure adherence to all relevant industry standards and regulatory requirements (e.g., ISO 9001).
• Champion a culture of quality throughout the organization, promoting continuous improvement and defect reduction.

Qualifications:

• Bachelor's degree in Engineering, Manufacturing Technology, or a related field.
• Minimum of 7 years of experience in quality control within a manufacturing environment.
• Proven expertise in quality management systems (QMS) and Lean Six Sigma principles.
• Strong knowledge of SPC, FMEA, and other quality tools.
• Experience with various inspection techniques and measurement equipment.
• Excellent analytical, problem-solving, and decision-making skills.
• Proficiency in data analysis software and reporting tools.
• Strong leadership and communication skills, with the ability to influence stakeholders at all levels.
• Experience in the electronics or precision machinery manufacturing sector is highly desirable.
• Ability to work effectively both independently and as part of a hybrid team.

This hybrid position requires a commitment to on-site presence for key inspections and team collaborations, with flexibility for remote work on specific tasks. Our client values innovation, integrity, and a relentless pursuit of excellence. Join a company that is shaping the future of manufacturing and contribute to building world-class products. This role offers competitive compensation, comprehensive benefits, and significant opportunities for career advancement within a thriving organization.

Our client, a leading innovator in advanced materials manufacturing, is seeking a highly skilled Remote Manufacturing Quality Control Engineer to join their esteemed team. This is a fully remote opportunity, enabling you to contribute to our quality assurance efforts from anywhere in the US. You will be responsible for developing, implementing, and maintaining comprehensive quality control systems and procedures throughout the manufacturing process. Your core duties will include analyzing production data, identifying quality issues, and implementing corrective and preventive actions (CAPA) to ensure products meet stringent standards. You will conduct root cause analysis for non-conformances, collaborate with production and engineering teams to resolve quality challenges, and ensure compliance with industry-specific quality regulations (e.g., ISO). The ideal candidate will possess a Bachelor's degree in Engineering (Mechanical, Industrial, or a related field) or Quality Management, with at least 5 years of experience in quality control within a manufacturing environment. Proven expertise in statistical process control (SPC), Six Sigma methodologies, and quality management systems is essential. Strong analytical, problem-solving, and communication skills are required to effectively work with remote teams and stakeholders. Experience with quality assurance software and testing equipment is a plus. This role offers an exceptional chance to drive product quality and operational excellence in a remote setting, contributing significantly to the company's reputation for delivering high-quality manufactured goods. You will be instrumental in upholding our commitment to superior product performance and customer satisfaction.

**Senior Quality Assurance Specialist - Sterile Manufacturing**
**Location:** Morrisville, NC
**Schedule:** Monday-Friday, 8:00 AM - 5:00 PM
**Pay Rate:** $35-$45/hour
**Type:** 6-Month Contract (Fully Benefited)
**Job Summary:**
**This on-site position is responsible for driving quality and compliance initiatives within a sterile pharmaceutical manufacturing environment. The Senior Quality Assurance (QA) Specialist ensures compliance with cGMP regulations and internal procedures by performing document review, internal audits, visual inspection of sterile drug products, and contributing to continuous improvement efforts. This role plays a key part in maintaining a strong quality culture and supporting regulatory inspection readiness, particularly in environments requiring** **Grade C gowning and aseptic handling** **.**
**Key Responsibilities:**
+ Perform **quality review and approval** of GMP documentation, including batch records, logbooks, forms, protocols, and reports.
+ Issue and control GMP documents to support manufacturing operations in **sterile cleanroom environments** .
+ Conduct **visual inspections of parenteral drug products** (qualification required) for defects or particulate contamination.
+ Execute internal audits and support external **client and regulatory inspections** .
+ Maintain and update quality databases and ensure proper document control.
+ Provide floor support to manufacturing teams and guide adherence to **aseptic techniques** and cleanroom behavior.
+ Assist in the development and revision of **SOPs, forms, and quality procedures** to meet regulatory standards and improve processes.
+ Collaborate cross-functionally to support batch review, deviation resolution, CAPAs, training, and vendor qualification efforts.
+ Serve as a mentor or resource for less experienced QA team members.
**Qualifications:**
+ Bachelor's degree in Chemistry, Biology, or a related field; Master's degree preferred.
+ Minimum **5+ years of GMP experience** in quality assurance, preferably in sterile manufacturing.
+ Familiarity with **Annex 1** , aseptic processing, and **Grade C gowning** requirements.
+ Ability to meet **visual inspection standards** (20/20 corrected vision).
+ Strong understanding of FDA and international cGMP regulations.
+ Experience working in environments requiring strict contamination control.
**Work Conditions & Physical Requirements:**
+ Full-time, 100% on-site position.
+ Frequent standing, occasional sitting, walking, kneeling, or crouching.
+ Regular lifting of up to 10-25 lbs; occasional lifting of up to 50 lbs.
+ Exposure to cleanroom environments, moving equipment, potential chemical or biohazardous materials.
+ Use of **Personal Protective Equipment (PPE)** required (gowns, respirators, gloves, etc.).
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Job DescriptionJob Description

Quality Assurance Technician – Manufacturing (Temporary Assignment)

Location: Torrance, CA
Duration: 3-Month Temporary Assignment
Pay: $25–$28/hour

Are you detail-oriented with a passion for precision? Our manufacturing client is seeking a Quality Assurance Technician to ensure products meet the highest standards of quality and compliance. This role offers hands-on experience with in-process testing, product inspections, and supporting new product launches.

Key Responsibilities:

• Perform daily in-process and physical testing to verify compliance with quality standards.

• Inspect components and final products, recommending modifications to prevent defects.

• Assist in launching new products by providing testing support and improvement suggestions.

• Utilize precision measuring tools such as calipers, micrometers, verniers, pin gauges, height gauges, radius gauges, protractors, dial indicators, optical comparators, and coordinate measuring machines.

• Read and interpret blueprints, ensuring parts meet specifications.

• Document results and support quality improvement initiatives.

• Operate industrial trucks, forklifts, and man lifts safely; maintain required certifications.

Qualifications:

• 1+ year mechanical inspection/calibration experience in manufacturing; plastics processing or product assembly experience a plus.

• Proficient in blueprint reading and measurement standards.

• Intermediate computer skills in Microsoft Word, Excel, and PowerPoint; SAP knowledge .

• Strong problem-solving skills with the ability to analyze causes of failure.

• Ability to work at elevated heights and handle industrial equipment safely.

Interested? Contact Daisy  at  or email for more information.

Company DescriptionKelly helps companies recruit and manage skilled workers and helps job seekers find great work in industries such as accounting and finance, education, engineering, government, manufacturing and production, technology, and more.

Since inventing the staffing industry in 1946, we’ve become experts in the many specialties and local and global markets we serve. With a network of suppliers and partners around the world, we connect 450,000+ people with work every year. We ensure companies have the people they need, when and where they’re needed most.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of , , , , , , , , veteran status, , marital status, , genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.Company DescriptionKelly helps companies recruit and manage skilled workers and helps job seekers find great work in industries such as accounting and finance, education, engineering, government, manufacturing and production, technology, and more.

Since inventing the staffing industry in 1946, we’ve become experts in the many specialties and local and global markets we serve. With a network of suppliers and partners around the world, we connect 450,000+ people with work every year. We ensure companies have the people they need, when and where they’re needed most.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of , , , , , , , , veteran status, , marital status, , genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Manufacturing Quality Assurance Analyst I, Albuquerque, NM
Night Shift
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 Manufacturing Quality Assurance (MQA) Analyst I role is an entry-level, developmental position. The MQA Analyst I will collaborate with the manufacturing team to provide support in process oversight and first-level decision-making activities. A successful candidate will exhibit a strong safety-focused quality mindset, a capacity for critical thinking, and an aptitude for understanding written SOPs. The MQA Analyst I must communicate effectively during collaborations with production partners and escalate issues urgently to facilitate timely decisions on the path forward. The MQA Analyst I will routinely work collaboratively with management, frontline manufacturing and support group technicians, as well as with senior members of the MQA OTF team.
Responsibilities
+ Perform daily audits
+ Perform room inspections
+ Review documentation
+ Communicate effectively
+ Collaborate intra and interdepartmentally
+ Read/interpret SOPs to ensure compliance
+ Maintain up to date trainings
+ Other duties as assigned
Qualifications
+ High school diploma or general education degree (GED)
+ FDA manufacturing regulated industry experience in an aseptic manufacturing environment, preferred
+ Operations or quality assurance in any industry, preferred
Other Qualifications:
+ Must pass a background check
+ Must pass a drug screen
+ May be required to pass Occupational Health Screening
+ Must pass pre-employment assessment
+ Must be able to obtain and maintain gowning certification
+ Must be able to obtain and maintain media qualification
+ Must be able to wear a respirator
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
The essential physical demands will vary for each Curia position.
All positions may require regular or occasional lifting, pushing and pulling up to 10 pounds, frequently; up to 25 pounds occasionally; and up to 50 pounds infrequently. Additionally, all positions entail regular sitting, standing and reaching, with some roles requiring prolonged periods of time for each activity. Visual acuity, both close and distant, along with depth perception is necessary in each role, with or without corrective lenses. Please note that employees are prohibited from wearing contact lenses in work areas with exposure to cleaning agents. Hand and finger dexterity are integral to all positions, with specific activities varying from typing to manipulating maintenance tools or operating keypads, switches, and buttons. Occasional stooping, kneeling, twisting, crouching, crawling and balancing are also part of each position's physical requirements. Certain roles may involve climbing and working at elevated heights as well.
Work Environment:
The work environment characteristics, described below, are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
The working environments will vary for each Curia position. The employee may be required to work in an office, manufacturing, or warehouse environment. The office environment is designed for comfort and productivity, with room temperature settings maintained for optimal working conditions. It is common to hear conversational noise in the background. The pharmaceutical manufacturing environment is sterile. Therefore, aseptic gowning is required. Personal protective equipment (nitrile gloves, clean room socks, face-shields, safety glasses, aprons, steel-toed shoes and powered air purifying respirators) is necessary, depending upon the task at hand. The employee may be exposed to wet and/or humid conditions, confined areas, and refrigerator or freezer temperatures when working in a sterile environment. The warehouse environment is typically set at a controlled temperature but the employee may be exposed to refrigerator or freezer temperatures when retrieving materials.
Some positions may occasionally be exposed to moving mechanical parts, elevated heights, airborne particles, electrical activities and vibration. In addition, some positions may work with or be exposed to, compressed gases and must wear ear protection.
All environments may be subject to working with or being exposed to cleaning agents.
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