24,658 Pharmaceutical Technician jobs in the United States
Pharmaceutical Technician
Posted 2 days ago
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Job Description
Pharmaceutical Technician
Posted 12 days ago
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Job Description
Job Description
We are seeking a Pharmaceutical Quality Technician to perform equipment preparation, bulk drug formulation, and aseptic filling duties. The role involves accurately documenting data and completing batch records, as well as performing cleaning and sanitization duties in compliance with applicable procedures. You will also need to successfully complete the facility's aseptic gowning and manufacturing qualification program and perform duties in ISO 5 (Grade A) and ISO 7 (Grade C) cleanrooms.
+ These positions are for off-shift roles.
+ Week 1 schedule: Thursday to Sunday from 6 PM to 6 AM.
+ Week 2 schedule: Friday to Sunday from 6 PM to 6 AM
+ Following a 48/36 hour rotation.
Responsibilities
+ Perform equipment preparation, bulk drug formulation, and aseptic filling duties.
+ Accurately document data and complete batch records.
+ Execute cleaning and sanitization duties as instructed by the applicable procedure.
+ Complete the facility's aseptic gowning and manufacturing qualification program.
+ Operate within ISO 5 (Grade A) and ISO 7 (Grade C) cleanrooms following cGMP regulations.
Essential Skills
+ Bachelor's degree in Science field (Biology, Chemistry, Health Sciences, Microbiology, etc.)
Pay and Benefits
The pay range for this position is $ - $ /yr.
MEDICAL BENEFITS starting day 1: Blue Cross Blue Shield medical and dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying for 75% of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!
Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!
PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!
WELLNESS TIME OFF: Employees earn 1 hour of time off for every 30 hours worked to use how you choose.
PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!
Workplace Type
This is a fully onsite position in Grand Rapids,MI.
Application Deadline
This position is anticipated to close on Oct 10, 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.
Manufacturing Pharmaceutical Technician
Posted 11 days ago
Job Viewed
Job Description
Assignment Description:
Manufacturing Pharmaceutical Technician
(Granulation/Blend/Bead Coating)
Onsite - 2nd shift (4pm- 2:30am, M-Th)
Job Summary
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines.
Primary Responsibilities
Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.
Prepare raw materials, blends, and bulk accountability throughout manufacturing processes.
Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging.
Identify, report, and resolve quality issues.
Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing equipment (oral solid dose manufacturing may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.).
Perform in-process testing and inspections as required by Master Batch Record (weighing, tablet thickness, tablet hardness, friability, visual inspection, etc.).
Clean and sanitize manufacturing rooms including walls, floors, and ceilings per SOPs.
Report accidents and unsafe conditions or unusual circumstances to supervisor.
Complete accurate and timely documentation. Follow good documentation practices in accordance with GMP.
Actively participate in Production team and Site communication meetings.
Maintain regular and punctual attendance; work overtime as required.
Support GMP investigations and events.
Identify and report potential GMP impacting situations.
Contribute to Standard Operating Procedure (SOP) writing in your technical area.
Education and Experience Requirements
High School Diploma or equivalent.
Up to three years pharmaceutical industry experience preferred or an equivalent combination of education, demonstrated mechanical skill, and experience in a similar industry.
Necessary Knowledge, Skills, and Abilities
General ability to perform basic to complex mathematical computations of addition, subtraction, multiplication, and division. Understanding of the Metric System of Measurement.
Preferred experience in oral solid dose (OSD) pharmaceutical manufacturing Granulation/Blending and Bead Coating operations.
Supervisor Responsibilities (if applicable)
The Pharmaceutical Technician has no direct reports.
Additional Information/General/Organizational
Quality/Compliance: Achieve a standard of excellence with work processes and outcomes while maintaining compliance with policies and all regulatory requirements.
Communication: Clear, accurate, effective and timely written and verbal communication. Strong attention to detail and ability to write and record data legibly and accurately in accordance to cGMP regulations.
Teamwork/Collaboration: Work effectively with others to achieve goals, build strong working relationships and a positive work environment.
Critical thinking/problem solving: general ability to collect, organize and analyze data. Ability to recognize, analyze and solve a variety of problems.
Initiative: Ability to take ownership of work, doing what is needed without being asked and appropriate follow-through.
Adaptability: Being receptive to feedback, willingness to learn, and open to continuous improvement.
Operational Excellence: Embrace and support Operational Excellence Culture and Initiatives.
Accountability: Demonstrate ambition and discipline to achieve organizational and career goals
Availability: To work site schedule of 10.5 hours a day, Monday-Thursday and overtime as needed.
Physical and Environmental Requirements
Occasionally move/traverse, ascend/descend step ladders, stairs, and/or platforms.
Wear appropriate Personal Protective Equipment including PAPR (Powered Air Purifying Respirator).
Occasionally, transport materials using manual and power assisted vehicles including manually pushing and pulling drums, totes, boxes, and pallets.
Lift and maneuver empty drums weighing up to 40 pounds up to five times per day; push and maneuver drums containing product weighing up to 275 pounds up to five times per day.
Perform cleaning and assembly/disassembly on production equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts may weigh up to 50 pounds.
Ability to work a 10 hour per day/4-day work week; 40 hours per week with overtime as required.
Assignment Description:
Manufacturing Pharmaceutical Technician
(Granulation/Blend/Bead Coating)
Onsite - 2nd shift (4pm- 2:30am, M-Th)
Job Summary
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines.
Primary Responsibilities
Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.
Prepare raw materials, blends, and bulk accountability throughout manufacturing processes.
Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging.
Identify, report, and resolve quality issues.
Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing equipment (oral solid dose manufacturing may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.).
Perform in-process testing and inspections as required by Master Batch Record (weighing, tablet thickness, tablet hardness, friability, visual inspection, etc.).
Clean and sanitize manufacturing rooms including walls, floors, and ceilings per SOPs.
Report accidents and unsafe conditions or unusual circumstances to supervisor.
Complete accurate and timely documentation. Follow good documentation practices in accordance with GMP.
Actively participate in Production team and Site communication meetings.
Maintain regular and punctual attendance; work overtime as required.
Support GMP investigations and events.
Identify and report potential GMP impacting situations.
Contribute to Standard Operating Procedure (SOP) writing in your technical area.
Education and Experience Requirements
High School Diploma or equivalent.
Up to three years pharmaceutical industry experience preferred or an equivalent combination of education, demonstrated mechanical skill, and experience in a similar industry.
Necessary Knowledge, Skills, and Abilities
General ability to perform basic to complex mathematical computations of addition, subtraction, multiplication, and division. Understanding of the Metric System of Measurement.
Preferred experience in oral solid dose (OSD) pharmaceutical manufacturing Granulation/Blending and Bead Coating operations.
Supervisor Responsibilities (if applicable)
The Pharmaceutical Technician has no direct reports.
Additional Information/General/Organizational
Quality/Compliance: Achieve a standard of excellence with work processes and outcomes while maintaining compliance with policies and all regulatory requirements.
Communication: Clear, accurate, effective and timely written and verbal communication. Strong attention to detail and ability to write and record data legibly and accurately in accordance to cGMP regulations.
Teamwork/Collaboration: Work effectively with others to achieve goals, build strong working relationships and a positive work environment.
Critical thinking/problem solving: general ability to collect, organize and analyze data. Ability to recognize, analyze and solve a variety of problems.
Initiative: Ability to take ownership of work, doing what is needed without being asked and appropriate follow-through.
Adaptability: Being receptive to feedback, willingness to learn, and open to continuous improvement.
Operational Excellence: Embrace and support Operational Excellence Culture and Initiatives.
Accountability: Demonstrate ambition and discipline to achieve organizational and career goals
Availability: To work site schedule of 10.5 hours a day, Monday-Thursday and overtime as needed.
Physical and Environmental Requirements
Occasionally move/traverse, ascend/descend step ladders, stairs, and/or platforms.
Wear appropriate Personal Protective Equipment including PAPR (Powered Air Purifying Respirator).
Occasionally, transport materials using manual and power assisted vehicles including manually pushing and pulling drums, totes, boxes, and pallets.
Lift and maneuver empty drums weighing up to 40 pounds up to five times per day; push and maneuver drums containing product weighing up to 275 pounds up to five times per day.
Perform cleaning and assembly/disassembly on production equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts may weigh up to 50 pounds.
Ability to work a 10 hour per day/4-day work week; 40 hours per week with overtime as required.
Manufacturing Pharmaceutical Technician
Posted 11 days ago
Job Viewed
Job Description
- Job Summary
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines.
Primary Responsibilities
- Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.
- Prepare raw materials, blends, and bulk accountability throughout manufacturing processes.
- Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging.
- Identify, report, and resolve quality issues.
- Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing equipment (oral solid dose manufacturing may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.).
- Perform in-process testing and inspections as required by Master Batch Record (weighing, tablet thickness, tablet hardness, friability, visual inspection, etc.).
- Clean and sanitize manufacturing rooms including walls, floors, and ceilings per SOPs.
- Report accidents and unsafe conditions or unusual circumstances to supervisor.
- Complete accurate and timely documentation. Follow good documentation practices in accordance with GMP.
- ctively participate in Production team and Site communication meetings.
- Maintain regular and punctual attendance; work overtime as required.
- Support GMP investigations and events.
- Identify and report potential GMP impacting situations.
- Contribute to Standard Operating Procedure (SOP) writing in your technical area.
- High School Diploma or equivalent.
- Up to three years pharmaceutical industry experience preferred or an equivalent combination of education, demonstrated mechanical skill, and experience in a similar industry.
- General ability to perform basic to complex mathematical computations of addition, subtraction, multiplication, and division. Understanding of the Metric System of Measurement.
- Preferred experience in oral solid dose (OSD) pharmaceutical manufacturing Granulation/Blending and Bead Coating operations.
The Pharmaceutical Technician has no direct reports.
dditional Information/ General/Organizational- Quality/Compliance: Achieve a standard of excellence with work processes and outcomes while maintaining compliance with policies and all regulatory requirements.
- Communication: Clear, accurate, effective and timely written and verbal communication. Strong attention to detail and ability to write and record data legibly and accurately in accordance to cGMP regulations.
- Teamwork/Collaboration: Work effectively with others to achieve goals, build strong working relationships and a positive work environment.
- Critical thinking/problem solving: general ability to collect, organize and analyze data. Ability to recognize, analyze and solve a variety of problems.
- Initiative: Ability to take ownership of work, doing what is needed without being asked and appropriate follow-through.
- daptability: Being receptive to feedback, willingness to learn, and open to continuous improvement.
- Operational Excellence: Embrace and support Operational Excellence Culture and Initiatives.
- ccountability: Demonstrate ambition and discipline to achieve organizational and career goals
- vailability: To work site schedule of 10.5 hours a day, Monday-Thursday and overtime as needed.
- Occasionally move/traverse, ascend/descend step ladders, stairs, and/or platforms.
- Wear appropriate Personal Protective Equipment including PAPR (Powered Air Purifying Respirator).
- Occasionally, transport materials using manual and power assisted vehicles including manually pushing and pulling drums, totes, boxes, and pallets.
- Lift and maneuver empty drums weighing up to 40 pounds up to five times per day; push and maneuver drums containing product weighing up to 275 pounds up to five times per day.
- Perform cleaning and assembly/disassembly on production equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts may weigh up to 50 pounds.
- bility to work a 10 hour per day/4-day work week; 40 hours per week with overtime as required.
- Summary of Work:
Role: Pharmaceutical Technician Mfg. Granulation, Blending and Bead Coating (we would like to see candidate with experience in bead coating and/or granulation and blending (in this order) .
Shift: 2 nd shift M-Th 4pm - 2:30 am
Length of contract: 6 months- 12 months
Note from HM: highlighting the candidates with resumes indicating OSD experience, however their organizations do not have these capabilities. Please submit resumes if they have actual granulation experience. PLEASE DO NOT COPY AND PASTE IN RESUME FROM JOB DESCRIPTION. MUST HAVE ACTUAL GRANULATION EXPERIENCE.
Manufacturing Pharmaceutical Technician
Posted 11 days ago
Job Viewed
Job Description
Location: Wilson,NC
Duration:- 8+ Months
Pay Rate: $21 to 23/hr
(Granulation/Blend/Bead Coating)
Onsite - 2nd shift (4pm- 2:30am, M-Th)
Summary of Work:
Role: Pharmaceutical Technician Mfg. Granulation, Blending and Bead Coating (we would like to see candidate with experience in bead coating and/or granulation and blending (in this order) .
Shift: 2nd shift M-Th 4pm - 2:30 am
Length of contract: 6 months- 12 months
Note from HM: highlighting the candidates with resumes indicating OSD experience, GRANULATION EXPERIENCE.
Job Summary
The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines.
Primary Responsibilities
- Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.
- Prepare raw materials, blends, and bulk accountability throughout manufacturing processes.
- Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging.
- Identify, report, and resolve quality issues.
- Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing equipment (oral solid dose manufacturing may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.).
- Perform in-process testing and inspections as required by Master Batch Record (weighing, tablet thickness, tablet hardness, friability, visual inspection, etc.).
- Clean and sanitize manufacturing rooms including walls, floors, and ceilings per SOPs.
- Report accidents and unsafe conditions or unusual circumstances to supervisor.
- Complete accurate and timely documentation. Follow good documentation practices in accordance with GMP.
- Actively participate in Production team and Site communication meetings.
- Maintain regular and punctual attendance; work overtime as required.
- Support GMP investigations and events.
- Identify and report potential GMP impacting situations.
- Contribute to Standard Operating Procedure (SOP) writing in your technical area.
High School Diploma or equivalent.
Up to three years pharmaceutical industry experience preferred or an equivalent combination of education, demonstrated mechanical skill, and experience in a similar industry.
Necessary Knowledge, Skills, and Abilities
General ability to perform basic to complex mathematical computations of addition, subtraction, multiplication, and division. Understanding of the Metric System of Measurement.
Preferred experience in oral solid dose (OSD) pharmaceutical manufacturing Granulation/Blending and Bead Coating operations.
Supervisor Responsibilities (if applicable)
The Pharmaceutical Technician has no direct reports.
Additional Information/General/Organizational
• Quality/Compliance: Achieve a standard of excellence with work processes and outcomes while maintaining compliance with policies and all regulatory requirements.
• Communication: Clear, accurate, effective and timely written and verbal communication. Strong attention to detail and ability to write and record data legibly and accurately in accordance to cGMP regulations.
• Teamwork/Collaboration: Work effectively with others to achieve goals, build strong working relationships and a positive work environment.
• Critical thinking/problem solving: general ability to collect, organize and analyze data. Ability to recognize, analyze and solve a variety of problems.
• Initiative: Ability to take ownership of work, doing what is needed without being asked and appropriate follow-through.
• Adaptability: Being receptive to feedback, willingness to learn, and open to continuous improvement.
• Operational Excellence: Embrace and support Operational Excellence Culture and Initiatives.
• Accountability: Demonstrate ambition and discipline to achieve organizational and career goals
• Availability: To work site schedule of 10.5 hours a day, Monday-Thursday and overtime as needed.
Physical and Environmental Requirements
- Occasionally move/traverse, ascend/descend step ladders, stairs, and/or platforms.
- Wear appropriate Personal Protective Equipment including PAPR (Powered Air Purifying Respirator).
- Occasionally, transport materials using manual and power assisted vehicles including manually pushing and pulling drums, totes, boxes, and pallets.
- Lift and maneuver empty drums weighing up to 40 pounds up to five times per day; push and maneuver drums containing product weighing up to 275 pounds up to five times per day.
- Perform cleaning and assembly/disassembly on production equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts may weigh up to 50 pounds.
- Ability to work a 10 hour per day/4-day work week; 40 hours per week with overtime as required.
Clean Room Pharmaceutical Technician
Posted 3 days ago
Job Viewed
Job Description
Job Description
Join our team as a Clean Room Pharmaceutical Technician on the 2nd Shift, working from 1pm to 11:30pm, Sunday through Wednesday. This role involves operating production equipment, including non-sterile filling machines, and packaging and labeling machines. You will ensure the supply of materials to assigned positions, clean equipment and production areas, and inspect parts following standard operating procedures. This position is key in troubleshooting basic issues and may involve providing training to others.
Responsibilities
+ Operate assigned equipment appropriately, including setup, operation, and cleaning of equipment and parts, ensuring configurations are correct and issues are communicated immediately.
+ Complete and review area production documentation, ensuring all entries are accurate, recorded in real time, and signed upon completion.
+ Maintain open communication with management regarding production updates, including deviations and corrective measures.
+ Exchange work status information within the department, management, and co-workers.
+ Maintain a clean work environment using appropriate cleaning solutions and prescribed methods and schedules.
+ Ensure designated equipment/tools are cleaned and sanitized according to established methods and schedules.
+ Clean and sanitize required glassware, completing wash documentation per SOP.
+ Handle raw materials and components according to prescribed methods, including procurement, weighing, verification, and formulation of solutions.
+ Maintain Aseptic Process Area sterile gowning qualifications.
+ Respond to equipment alarms or malfunctions immediately, communicating conditions to subject matter experts.
+ Assist co-workers in the production of finished products within time limits outlined in SOPs and/or manufacturing instructions.
+ Receive and ship plant uniforms and scrub uniforms for cleaning, stock garments and supplies for clean rooms and sterile core, and prepare garments for sterilization.
+ Assist with special projects as required or requested.
+ Promote a safe and harmonious work environment.
+ Maintain compliance with SOPs, GMPs, and all company policies.
Essential Skills
+ Associate or Bachelor's Degree from a regionally accredited institution.
+ One or more years of previous work experience in a hospital or manufacturing environment, preferably in a clean room setting.
+ Basic mechanical skills related to the operation of equipment.
+ Knowledge and skill in operating specialized equipment, such as filling, wash, and sanitizing equipment.
+ Skill in handling multiple projects or tasks simultaneously.
+ Advanced problem safety sensitivity and the ability to recognize safety issues.
+ Skill in time management and attention to detail.
+ Skill in math, with an understanding of measurements and conversions.
+ Skill in communicating professionally with coworkers and management.
+ Ability to apply critical thinking and maintain confidentiality.
Additional Skills & Qualifications
+ Knowledge of clean room procedures and GMP regulations, preferred but not required.
+ Experience with general computer functions such as Microsoft Office programs and spreadsheets.
+ Ability to follow personal hygiene standards and wear protective attire as required.
+ Ability to be flexible with work hours and provide motivational support.
Work Environment
This role requires working in a clean room, lab, and production environment. The position involves wearing protective attire as required and adhering to strict safety and hygiene standards. The shift schedule is 2nd Shift, from 1pm to 11:30pm, Sunday through Wednesday.
Pay and Benefits
The pay range for this position is $24.00 - $26.60/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 Syracuse,NY.
Application Deadline
This position is anticipated to close on Oct 20, 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.
Pharmaceutical Manufacturing Technician
Posted today
Job Viewed
Job Description
Pharmaceutical Manufacturing Technician
W2 Contract
Salary Range: $47,840 - $56,160 per year
Location: San Carlos, CA - Onsite Role
Duties and Responsibilities:
- Perform daily manufacturing tasks as assigned by the supervisor.
- Weigh materials, prepare solutions, and production materials.
- Perform manufacturing, packaging, and related tasks.
- Document production activities in manufacturing batch records.
- Clean up the production equipment and the production area.
- Clean and prepare manufacturing equipment
Requirements and Qualifications:
- Minimum High School Diploma or GED and three (3) to five (5) years related experience in a GMP pharmaceutical manufacturing environment.
- Experience with analytical balances, weighing materials accurately
- Experience with handling of solids and liquids, pouring, and filtering.
Desired Skills and Experience
Manufacturing, Pharmaceutical, Packaging, GMP
Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate.
Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at
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Pharmaceutical Manufacturing Technician
Posted 2 days ago
Job Viewed
Job Description
Job Description
- Generate, assist and execute documentation associated with manufacture, Batch Documents, Log Books, Labels, check sheets , protocols, Change control, QTS etc
- Complete complex bulk product manufacturing activities to convert incoming raw materials into intermediate product
- Complete complex processing of intermediate bulk to convert this to a final patient ready final presentation
- Set up complex manufacturing equipment, manage and check documentation generated.
- Complete activities associated with the operation and maintenance of a classified manufacturing space
- Complete activities identified as operator care tasks associated with the maintenance and operation of complex manufacture equipment.
- Generate, manage and report operational performance associated data
- Identify, own and lead continuous improvement based projects
Qualifications:
Qualifications
- High school diploma
- Must hold a valid driver’s license
- Pharmaceutical manufacturing experience is a plus
- Role requires a Groton site presence. The job requires the operation of manufacturing equipment in the Groton manufacturing area. Standing, bending, climbing, reaching, and lifting upward of 55 pounds may be required. Personal Protective Equipment such as gloves, a full Tyvek suit and breathable air and/or filtering face piece is often required.
- Must be able to wear appropriate PPE (i.e. daily uniform, safety glasses, respirators and full protective suits) when necessary
- Strong computer, scientific, and organizational skills
- Excellent communication (oral and written) and attention to detail
- Ability to perform heavy lifting (up to 55lbs)
- Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
- Strong computer, scientific, and organizational skills
- Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
- Position is full-time, Monday-Friday, 8:00 am - 5:00 pm.
- Candidates currently living within a commutable distance of Groton, CT are encouraged to apply
- Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
- #LI-EB1
- Authorization to work in the United States indefinitely without restriction or sponsorship
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Compensation:
$18-$18
Pharmaceutical Manufacturing Technician
Posted 3 days ago
Job Viewed
Job Description
Pharmaceutical Manufacturing Technician
W2 Contract
Salary Range: $47,840 - $56,160 per year
Location: San Carlos, CA - Onsite Role
Duties and Responsibilities:
- Perform daily manufacturing tasks as assigned by the supervisor.
- Weigh materials, prepare solutions, and production materials.
- Perform manufacturing, packaging, and related tasks.
- Document production activities in manufacturing batch records.
- Clean up the production equipment and the production area.
- Clean and prepare manufacturing equipment
Requirements and Qualifications:
- Minimum High School Diploma or GED and three (3) to five (5) years related experience in a GMP pharmaceutical manufacturing environment.
- Experience with analytical balances, weighing materials accurately
- Experience with handling of solids and liquids, pouring, and filtering.
Desired Skills and Experience
Manufacturing, Pharmaceutical, Packaging, GMP
Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate.
Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at .
Pharmaceutical Manufacturing Technician
Posted 11 days ago
Job Viewed
Job Description
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, age, disability, marital status, citizenship, national origin, genetic information, protected veteran status or any other characteristic protected by federal, state, or local law.
About the Organization
Mikart is a contract development and manufacturing organization (CDMO) supplying a comprehensive suite of services across the drug development and commercialization continuum. Wherever you are in the journey from conceptualization to maximizing market adoption, Mikart is your seasoned industry partner - we've been delivering the highest quality products surpassing the most exacting client standards for over 45 years.
Category
Manufacturing
Description
The Pharmaceutical Manufacturing Technician is responsible for dispensing prescribed amounts of raw material for use in manufacturing; granulating, drying, blending, liquid manufacturing and coating duties performed as part of the process of generating quality products.
Duties include the following:
- Maintaining the pharmacy and manufacturing areas and equipment in a clean, neat and orderly manner.
- Requisitioning materials needed from warehouse. Verifying all materials received are correct, released, and within the expiry period.
- Weighing raw materials according to master records and record all dispensing information in an accurate and timely manner. Dispensing material on a first in/first out basis. Labeling all containers appropriately.
- Cleaning all areas and equipment to be used. Completing appropriate logbooks prior to requesting Quality Assurance clearance.
- Verifying that all necessary materials are correct, present, and released. Obtaining supervisory verification of all weights and measurements to assure correctness of quantities and calculations prior to processing. Assuring that all outer containers are free from dust and debris.
- Processing raw materials according to instructions, documenting all required actions in the master records. Operating all equipment in a safe manner according to established procedures.
- Performing in-process testing as required in the master instructions, and document appropriately. Monitoring the product being processed to assure compliance with all in-process specifications.
- Weighing and documenting yield for all products after completion. Labeling all product containers and reject materials appropriately.
- Transferring completed products to the proper in-process quarantine area or processing area as appropriate.
- Cleaning the manufacturing areas and equipment promptly at the conclusion of each operation. Cleaning hoses used to transfer purified water according to schedule. Sanitizing the floor drains according to schedule.
Key Characteristics
- The individual selected for this role must like working in a fast paced but highly compliant environment.
- Team player.
- Reliable, self-starting, and organized.
- Able to follow clear instructions.
- Attention to detail.
- Robust communication skills (oral and written).
- Flexible work hours.
- High School diploma or equivalent, with good mathematical skills.
- Experience in food or pharmaceutical manufacturing a plus.
- Experience in a manufacturing facility in compliance with 21CFR Part 211--cGMP is preferred
- Fluency in the English language is required.
- Must be able to life at least 65 lbs
- Must be able to perform required repetitive lifting tasks.
- Lifting, walking, repetitive hand motions and attentiveness required.
- Climb ladders and stairs, walking, bending, stooping is required.
- Occasional heavy lifting or moving required.
- The ability to gown and work successfully in a clean room environment.
- The ability to wear a respirator if required.
Salary
Mikart, LLC offers a competitive compensation program and comprehensive benefits package to our employees.
This position is currently accepting applications.