22 Measuring Dosages jobs in the United States

Pharmaceutical Technician

13203 Syracuse, New York Actalent

Posted 2 days ago

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Job Description

Pharmaceutical Production Operations Specialist include:
+ Operate technically sophisticated equipment through HMIs.
+ Performs machine set-up, operation, and troubleshooting on various pieces of packaging equipment.
+ Diagnose and repair issues with mechanical and electrical operations of equipment.
+ Set-up, monitor, adjust, and program packaging equipment within approved procedural and GMP guidelines.
+ Clean work area and equipment with various cleaning aids such as wipes, brooms/mops following standard operating procedures.
+ Maintain documentation of inspections and cleaning including logbooks and batch record documents.
+ Analyze conditions/issues using analytical skills to develop a solution.
+ Assists management with data analysis, report writing, investigations, and other tasks as assigned.
+ Assist in team development by training, mentoring, coaching.
+ Candidates should be mechanically inclined self-starters with a strong attention to detail and must be available for overtime and/or additional days per week.
Knowledge, Skills & Abilities:
+ Knowledge of contemporary electrical and mechanical technologies and packaging.
+ Knowledge of production maintenance practices and procedures.
+ Knowledge and skill in operating various specialized equipment.
+ Knowledge and skill in interpersonal communications including coaching, counseling, and providing leadership to team.
+ Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
+ Ability to effectively present information and respond to questions from managers, coworkers, and other individuals.
+ Demonstrates flexible and efficient time management and ability to prioritize workload.
+ Ability to pay close attention to detail and coordinate various activities simultaneously.
+ Adhere to Company Policy and Procedures.
Required Education, Experience:
+ Associate degree in electrical and mechanical technologies, or equivalent combination of experience and education. 3-5 years' experience in a similar field with background in pharmaceutical manufacturing, equipment maintenance, or equivalent combination of training/experience.
+ Typical 3rd shift production schedule is 4, 10-hour days. Must be available for various days of the week and a 5-day schedule as indicated. Overtime rates apply to hours over 40 per week.
+ Standard work hours for 3rd shift are 8:00 PM - 6:30 AM. Alternative work hours/work schedule may be required at the discretion of management. A 15% differential for working on 3rd shift. Training will occur on 1st shift.
+ Compensation: Rate is commensurate with experience, starting at $25/hr.
?Required qualifications:
+ Legally authorized to work in the United States
+ 18 years or older
Pay and Benefits
The pay range for this position is $5760.00 - 47840.00/yr.
Eligibility requirements apply to some benefits and may depend on your jobclassification and length of employment. Benefits are subject to change and may besubject to specific elections, plan, or program terms. If eligible, the benefitsavailable 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 Jul 29, 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.
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Pharmaceutical Technician

13203 Syracuse, New York Actalent

Posted 9 days ago

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Job Description

Vial Fill Technician
Job Description
We are seeking a Pharmaceutical Technician working 4 x 10-hour shifts. This position operates production equipment, including non-sterile filling machines, and packaging and labeling machines. You will be responsible for supplying materials to assigned positions, cleaning equipment and production areas, and inspecting parts/items following standard operating procedures. The role also includes troubleshooting basic issues and assisting in training.
Responsibilities
+ Operate all assigned equipment appropriately and per established methods and procedures, including setup, operation, and cleaning of equipment and parts.
+ Confirm configurations are correct, check for leaks or other abnormalities, and ensure proper communication of any issues immediately.
+ Complete operational documentation per SOP and tag/palletize/place all returned and rejected items as needed.
+ Review area production documentation and verify all documented entries are accurate, recorded in real time, and signed as completed.
+ Maintain open lines of communication with management, informing them of production updates, including deviations and corrective measures.
+ Exchange work status information within the department, management, and co-workers.
+ Maintain a clean environment/work area using appropriate cleaning solutions and prescribed methods and schedules.
+ Ensure designated equipment/tools are cleaned and sanitized appropriately per established methods and schedules.
+ Clean and sanitize required glassware by loading glassware into washers and completing wash documentation per SOP.
+ Handle raw materials and components appropriately according to prescribed methods and procedures, including procurement, weighing, verification, dispensing, and formulating solutions.
+ Maintain Aseptic Process Area sterile gowning qualifications.
+ Respond immediately to equipment alarms or malfunctions by identifying alarm conditions and communicating them to subject matter experts.
+ Assist co-workers in the production of finished products within the time limits outlined in SOPs and/or manufacturing instructions.
+ Receive and ship all plant uniforms and scrub uniforms for cleaning.
+ Receive and stock all garments and supplies for clean rooms and sterile core, and prepare all garments to be shipped and sterilized.
+ Assist with special projects as required or requested.
+ Promote a safe and harmonious work environment.
+ Maintain compliance with SOPs, GMPs, and all company policies.
+ Perform other duties as assigned.
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, or in clean room filling
+ Experience working in a production environment, ideally in a clean room setting
+ Basic mechanical skills related to the operation of equipment
+ Knowledge and skill in operating various specialized equipment, such as filling, wash, and sanitizing equipment
+ Knowledge of clean room procedures
+ Knowledge of and compliance with GMP (Good Manufacturing Practices) regulations
+ Knowledge of general computer functions such as Microsoft Office programs and spreadsheets
+ Skill in handling several projects or tasks at the same time, or within a given time frame
+ Advanced problem safety sensitivity; the ability to recognize a safety issue or potential safety issue
+ Skill in using time management techniques in personal daily tasks and those of others
+ Skill in attention to detail and focus on quality, accuracy, sterility, and aseptic technique
+ Skill in communicating with coworkers, management team members, and other individuals in a courteous and professional manner
+ Skill in math with an understanding of measurements and conversions
+ Skill in recognizing deviations from procedures and anomalies and immediately communicating them
+ Ability to apply critical thinking
+ Ability to maintain confidentiality of all internal and external information and processes
+ Ability to follow personal hygiene standards/procedures according to SOP
+ Ability to wear protective attire as required and handle materials in the correct order per SOP
+ Ability to follow all appropriate SOPs and safety procedures per company guidelines
+ Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists
+ Ability to be flexible in work hours
+ Ability to provide motivational support
Additional Skills & Qualifications
+ Experience in a clean room setting preferred but not required
+ Knowledge of clean room procedures preferred but not required
+ Knowledge of GMP regulations preferred but not required
Work Environment
This position operates in a clean room, lab, and production environment. The work requires adherence to personal hygiene standards and wearing protective attire. The role involves handling specialized equipment and maintaining a sterile work area.
Pay and Benefits
The pay range for this position is $19.00 - $20.90/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 Jul 22, 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.
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Manufacturing Pharmaceutical Technician

27893 Wilsons Mills, North Carolina Axelon

Posted 12 days ago

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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.
    • 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.
  • 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
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Pharmaceutical Technician I

27835 Greenville, North Carolina Catalent Pharma Solutions

Posted 2 days ago

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Job Description

**Pharmaceutical Technician I**
**Position Summary**
Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. 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.
Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. 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 Pharmaceutical Technician I is responsible for the dispensing, compounding, compressing, encapsulating, tablet coating and printing of good manufacturing practice (GMP) commercial batches in an oral solid dosage (OSD) environment. The Pharmaceutical Technician I will work on a second shift schedule from 4 pm - 2:30 am. ?
This position is 100% on-site at the Greenville site.
**The Role**
+ With minimal oversight, assemble, disassemble, clean and store manufacturing equipment.
+ Assist with troubleshooting machinery and equipment and recommend corrective or preventative measures.
+ Ensure all batch records and logbook entries are accurately documented and compliant with SOPs and FDA cGMP guidelines.
+ With minimal supervision, conduct setup, changeover, and manufacturing activities with adherence to SOPs and safety requirements.
+ Other duties as assigned.
**The Candidate**
+ High school diploma or equivalent with at least 2 years of experience in pharmaceutical OSD manufacturing or
+ Associate degree with at least 1 year of experience in pharmaceutical OSD manufacturing.
+ Required to obtain internal forklift operation certification.
+ Position requires the ability to lift 50 lbs unassisted, and push and pull in excess of 100 lbs.
+ Majority of work day is performed while standing and walking.
+ Requires the use of hands for simple grasping and fine manipulations.
+ Ability to occasionally bend, stoop, twist, and have full range of motion in upper and lower extremities.
+ Exposure to hazardous chemicals, other active chemical ingredients, dust, fumes, gases, skin and respiratory irritants, moving machinery parts, and damp, humid and wet environments.
+ Must be able to use a variety of tools, equipment, and machinery.
**Why You Should Join Catalent**
+ Competitive medical benefits and 401K
+ 152 hours of PTO + 8 Paid Holidays
+ Dynamic, fast-paced work environment
+ Opportunity to work on Continuous Improvement Process
**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 ( .
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Aseptic Pharmaceutical Technician

13203 Syracuse, New York Actalent

Posted 3 days ago

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Job Description

Aseptic Pharmaceutical Technician
Job Description
As an Aseptic Pharmaceutical Technician, you will be responsible for performing all procedures and processes related to the filling of sterile products, ensuring the cleanliness of the aseptic process area. You will prepare components for use in sterile filling and set up and operate various equipment according to standard operating procedures. The role requires employing aseptic techniques while working in a clean room/ISO rated environment.
Responsibilities
+ Perform procedures and processes for the filling of sterile products.
+ Ensure cleanliness of the aseptic process area.
+ Set up and operate equipment such as filling machine, filler parts, powder recovery system, vial washer, and parts assembly pre-sterilization.
+ Employ aseptic techniques while working in a clean room/ISO rated environment.
+ Clean and sanitize walls, equipment, and floors following SOPs.
+ Perform preventative maintenance on equipment and replace damaged or worn parts.
+ Operate equipment like turntable, filling machine, sterilizing tunnel, vial washer, and conveyors according to SOP.
+ Operate autoclave to steam sterilize components and machine parts.
+ Obtain appropriate components per documentation and handle according to SOPs.
+ Participate in training programs to maintain qualification status in aseptic areas.
+ Qualify for Quality Control environmental monitoring tasks.
+ Interact with other technicians to learn processes.
Essential Skills
+ Mechanically inclined self-starter
+ Strong attention to detail
+ Availability for overtime and additional work days
+ Cleanroom knowledge
+ Data entry skills
+ Aseptic and aseptic technique
+ Sterile processing
+ Quality control
Additional Skills & Qualifications
+ High School Diploma or equivalent required
+ Associates Degree in Sciences or equivalent preferred
+ One to three years experience in a pharmaceutical or manufacturing environment
+ Prior experience in a regulated industry is a plus
+ On-site training provided
Work Environment
You will be working in a clean room environment. The position is available for the 3rd shift, which operates from 8:00 p.m. to 6:30 a.m., with a 15% pay differential. Candidates must be flexible to work additional days or hours. Initial orientation and on-the-job training occur during the 1st shift, from 6:00 a.m. to 4:30 p.m.
Pay and Benefits
The pay range for this position is $45760.00 - $47840.00/yr.
Eligibility requirements apply to some benefits and may depend on your jobclassification and length of employment. Benefits are subject to change and may besubject to specific elections, plan, or program terms. If eligible, the benefitsavailable 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 Jul 28, 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.
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Aseptic Pharmaceutical Technician

13203 Syracuse, New York Actalent

Posted 9 days ago

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Job Description

Aseptic Pharmaceutical Technician
Job Description
As an Aseptic Pharmaceutical Technician, you will be responsible for performing all procedures and processes related to the filling of sterile products, ensuring the cleanliness of the aseptic process area. You will prepare components for use in sterile filling and set up and operate various equipment according to standard operating procedures. The role requires employing aseptic techniques while working in a clean room/ISO rated environment.
Responsibilities
+ Perform procedures and processes for the filling of sterile products.
+ Ensure cleanliness of the aseptic process area.
+ Set up and operate equipment such as filling machine, filler parts, powder recovery system, vial washer, and parts assembly pre-sterilization.
+ Employ aseptic techniques while working in a clean room/ISO rated environment.
+ Clean and sanitize walls, equipment, and floors following SOPs.
+ Perform preventative maintenance on equipment and replace damaged or worn parts.
+ Operate equipment like turntable, filling machine, sterilizing tunnel, vial washer, and conveyors according to SOP.
+ Operate autoclave to steam sterilize components and machine parts.
+ Obtain appropriate components per documentation and handle according to SOPs.
+ Participate in training programs to maintain qualification status in aseptic areas.
+ Qualify for Quality Control environmental monitoring tasks.
+ Interact with other technicians to learn processes.
Essential Skills
+ Mechanically inclined self-starter
+ Strong attention to detail
+ Availability for overtime and additional work days
+ Cleanroom knowledge
+ Data entry skills
+ Aseptic and aseptic technique
+ Sterile processing
+ Quality control
Additional Skills & Qualifications
+ High School Diploma or equivalent required
+ Associates Degree in Sciences or equivalent preferred
+ One to three years experience in a pharmaceutical or manufacturing environment
+ Prior experience in a regulated industry is a plus
+ On-site training provided
Work Environment
You will be working in a clean room environment. The position is available for the 3rd shift, which operates from 8:00 p.m. to 6:30 a.m., with a 15% pay differential. Candidates must be flexible to work additional days or hours. Initial orientation and on-the-job training occur during the 1st shift, from 6:00 a.m. to 4:30 p.m.
Pay and Benefits
The pay range for this position is $45760.00 - $47840.00/yr.
Eligibility requirements apply to some benefits and may depend on your jobclassification and length of employment. Benefits are subject to change and may besubject to specific elections, plan, or program terms. If eligible, the benefitsavailable 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 Jul 22, 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.
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Pharmaceutical Manufacturing Technician

84193 Salt Lake City, Utah Aerotek

Posted today

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Job Description

Pharmaceutical Manufacturing Technician - Clean Room Technician

Salt Lake City, UT | $23–24/hr | 1st Shift: 6:00 AM – 2:30 PM (Mon–Fri)

Industry:Pharmaceutical Manufacturing |Contract through December 2025

Looking to grow your career in a clean, high-tech environment?

We’re hiring Pharmaceutical Manufacturing Technicians to join a leading pharmaceutical production team in Salt Lake City. This is a contract position through the end of the year, with potential for extension or long-term placement.

What You’ll Do:

  • Operate production equipment to manufacture delicate pharmaceutical products.

  • Measure, pour, and handle raw materials with precision.

  • Follow strict cleanroom protocols, including gowning and hygiene procedures.

  • Clean, sterilize, and maintain workstations and equipment.

  • Accurately follow batch records and standard operating procedures (SOPs).

  • Maintain a safe and organized work environment.

What We’re Looking For:

  • 1–2 years of experience in manufacturing, food production, or raw material handling.

  • High School Diploma, GED, or official transcripts required.

  • Comfortable working in aregulated, sterile environment.

  • Strong attention to detail and ability to follow written instructions.

  • Physically able to stand for long periods and perform repetitive tasks.

Why Join Us?

  • Stable, full-time hours in a clean, climate-controlled facility.

  • Gain valuable experience in the pharmaceutical industry.

  • Be part of a team that values safety, precision, and collaboration.

Pay and Benefits

The pay range for this position is $3.00 - 24.15/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 Salt Lake City,UT.

Application Deadline

This position is anticipated to close on Jul 31, 2025.

About Aerotek:

We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.

Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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Pharmaceutical Manufacturing Technician

30383 Atlanta, Georgia Mikart

Posted 19 days ago

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Job Description

EOE Statement
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.
Position Requirements

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.
Education and Qualifications
  • 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.
  • 1st and 2nd Shift openings
  • Must be able to work overtime if required
Physical Demands
  • 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 is required.


Salary
Mikart, LLC offers a competitive compensation program and comprehensive benefits package to our employees.

This position is currently accepting applications.
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Pharmaceutical Manufacturing Technician

84190 Salt Lake City, Utah Aerotek

Posted today

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Job Description

**Pharmaceutical Manufacturing Technician - Clean Room Technician**
? _Salt Lake City, UT_ | ? _$23-24/hr_ | ? _1st Shift: 6:00 AM - 2:30 PM (Mon-Fri)_
Industry:Pharmaceutical Manufacturing |Contract through December 2025
Looking to grow your career in a clean, high-tech environment?
We're hiring Pharmaceutical Manufacturing Technicians to join a leading pharmaceutical production team in Salt Lake City. This is a contract position through the end of the year, with potential for extension or long-term placement.
**What You'll Do:**
+ Operate production equipment to manufacture delicate pharmaceutical products.
+ Measure, pour, and handle raw materials with precision.
+ Follow strict cleanroom protocols, including gowning and hygiene procedures.
+ Clean, sterilize, and maintain workstations and equipment.
+ Accurately follow batch records and standard operating procedures (SOPs).
+ Maintain a safe and organized work environment.
**What We're Looking For:**
+ 1-2 years of experience in manufacturing, food production, or raw material handling.
+ High School Diploma, GED, or official transcripts required.
+ Comfortable working in aregulated, sterile environment.
+ Strong attention to detail and ability to follow written instructions.
+ Physically able to stand for long periods and perform repetitive tasks.
**Why Join Us?**
+ Stable, full-time hours in a clean, climate-controlled facility.
+ Gain valuable experience in the pharmaceutical industry.
+ Be part of a team that values safety, precision, and collaboration.
**Pay and Benefits**
The pay range for this position is $3.00 - 24.15/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 Salt Lake City,UT.
**Application Deadline**
This position is anticipated to close on Jul 31, 2025.
**About Aerotek:**
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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Pharmaceutical Manufacturing Technician I

99302 Pasco, Washington ZipRecruiter

Posted 11 days ago

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Job Description

Job DescriptionJob Description

Manufacturing Technician I  

THIS POSITION IS NOT ELIGIBLE FOR VISA SUPPORT OF ANY KIND, CURRENTLY OR IN THE FUTURE, AND SUCH SPONSORSHIP WILL NOT BE PROVIDED. 
 
Where science meets innovation, and YOU make the difference! 

About AustinPx 

At AustinPX, we’re not just advancing science—we’re accelerating it! We partner with the world's leading pharmaceutical companies to develop and deliver life-changing treatments to patients faster. And now, we’re on the hunt for fresh talent to help us on this mission and to develop into future pharmaceutical leaders! Ready to contribute to life-changing projects, and have a blast doing it? Then read on! 

AustinPx is a contract development and manufacturing organization (CDMO) specializing in preclinical through Phase II formulation and process development and GMP manufacturing of oral dosage forms. We specialize in bioavailability enhancement, including our next amorphous dispersion platform, KinetiSolTM Technology. At AustinPx, we recruit and develop exceptional individuals with a passion for science and determination to excel. We offer a technically challenging and stimulating environment and the opportunity to grow and advance in your career.  

AustinPx is committed to a culture of respect and excellence in everything we do.   As a customer-facing organization, we are laser focused on providing client-centric service. Serving our clients well goes beyond technical knowhow - it requires strong communication skills, a commitment to quality, integrity and respect for our colleagues and clients. We want people who are passionate about pharmaceutical development, have a sense of urgency, and enjoy solving problems. 

We offer a comprehensive suite of health and retirement benefits, resources and programs to meet your and your family’s needs. Our positive and fast-paced working environment is continually focused on improving processes to remain innovative and dynamic. 

Position Description 

The Manufacturing Technician I is responsible for production of pharmaceutical solid oral dosage forms for Phase I and II clinical trials. Under the direction of the Manufacturing Director or Supervisor, adhering to current Good Manufacturing Practices (cGMP) and following Standard Operating procedures (SOPs), the Manufacturing Technician will work hands-on in GMP production facility. Using a variety of compounding and manufacturing equipment and technologies, including blending, granulation, encapsulation, compression, and coating tools, you will: 

  • Responsible for manufacturing of cGMP (Good Manufacturing Practices) products, following SOP’s (Standard Operating Procedures), and providing accurate documentation in production batch records. 

  • Daily responsibilities vary and include equipment and room set up, breakdown and clean up, weighing of materials, running equipment, troubleshooting equipment, samples submission, and packaging. 

  • Operates automated or semi-automated equipment. 

  • Prepares materials and equipment for production. 

  • Supports equipment cleaning verification and validation activities. 

  • Assist with the warehouse, stocking, receiving, and shipping. 

  • Other duties as assigned. 

  • This is a full-time hourly position on 1st shift Monday-Friday with hours of 7:30am-4:00pm, though these hours may vary to meet the needs of the production schedule. 

What We’re Looking For: 

  • High School Diploma or GED equivalent is required. Prior coursework or experience working within a regulated environment (GMP/FDA/DEA/OSHA), is highly . 

  • Mechanical and technical aptitude and the desire to work in a regulated environment and strictly follow procedures is required to be successful in this position.   

  • Communication Skills: Ability to read, write, and comprehend reports, technical and cGMP documents as well as correspondence. 

  • There is no “i” in Team:  A team player with a positive attitude and able to take initiative. Strong attention to detail, safety, quality and client requirements is critical. Critical thinking skills with the ability to proactively point out areas for improvement or to avoid risks.  

  • Physical Requirements: This position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently. 

  • Cabbage: The annual pay range for this position is $40,000 – $46,000 annually. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc.  Relocation Assistance is NOT available for this position. 

Why AustinPX? 

  • Real Impact: Your work could play a part in getting life-saving medications to patients sooner. 

  • Mentorship: Learn from experts in the field (who also happen to be pretty awesome people). 

  • Work Hard, Play Hard: Enjoy fun team activities, such as corn-hole tournaments, movie day, floats on the river, and puzzles and board games.  

  • Career Growth: AustinPx offers rewarding opportunities to further your career! Individuals who show promise and a commitment to growth have the opportunity to expand their career. 

  • Benefits: Generous 401K match, Paid Time Off accrual, and 10+ paid holidays/year, Medical, Dental and Vision benefits.  Life Insurance, Short Term and Long Term also provided.  

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