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Pharmaceutical Production Associate Jobs (NOW HIRING)

Production Associate

Chandler, AZ · On-site

$14.75 - $18.75/hr

At least 2 years of experience in food, nutraceutical, pharmaceutical, or chemical manufacturing * GMP or cGMP experience preferred * Working knowledge of ERP systems for production tracking and ...

Production Associate

Buffalo, NY · On-site

$20 - $24/hr

Production Associate - Metal Polishing & Finishing Overview This is an entry‑level production ... pharmaceutical, and chemical equipment. We are open to candidates with strong mechanical aptitude ...

Deli Production Associate

Wauwatosa, WI · On-site

$14.50 - $18.50/hr

... ® portfolio of products, to locations in all 50 states. Our braggingly happy team members ... pharmacies and fuel centers. Ready to contribute to the success of our food solutions company?

Deli Production Associate

Wauwatosa, WI

$14.50 - $18.50/hr

... products, to locations in all 50 states. Our braggingly happy team members - ranging from bakery ... pharmacies and fuel centers. Ready to contribute to the success of our food solutions company?

Deli Production Associate

Madison, WI · On-site

$15 - $19.25/hr

... ® portfolio of products, to locations in all 50 states. Our braggingly happy team members ... pharmacies and fuel centers. Ready to contribute to the success of our food solutions company?

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Pharmaceutical Production Associate information

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$10

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How much do pharmaceutical production associate jobs pay per hour?

As of Jun 23, 2026, the average hourly pay for pharmaceutical production associate in the United States is $16.82, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $18.27 per hour, depending on experience, location, and employer.

What is the highest paying job in pharmaceuticals?

In pharmaceutical production, senior roles such as Pharmaceutical Manufacturing Director or Vice President of Manufacturing tend to be the highest paying positions, often earning six-figure salaries. These roles require extensive experience, leadership skills, and knowledge of regulatory compliance and production processes.

What is a pharmaceutical manufacturing associate?

A pharmaceutical manufacturing associate is a worker responsible for preparing, assembling, and monitoring the production of medications in a pharmaceutical facility. They follow strict safety and quality protocols, often operate specialized equipment, and may need certifications such as GMP (Good Manufacturing Practice) training. The role typically involves working in a clean environment and adhering to detailed procedures to ensure product safety and efficacy.

What does a Pharmaceutical Production Associate do?

A Pharmaceutical Production Associate is responsible for assisting in the manufacturing and packaging of pharmaceutical products in a controlled environment. Their duties often include operating machinery, measuring and mixing ingredients, following strict safety and quality protocols, and maintaining documentation for compliance. They work as part of a team to ensure products meet regulatory standards and are safely prepared for distribution. This role requires attention to detail, knowledge of good manufacturing practices (GMP), and adherence to health and safety regulations.

What is the role of a pharmaceutical production assistant?

A pharmaceutical production assistant supports the manufacturing of medications by preparing equipment, assembling components, and following strict safety and quality protocols. They often work under supervision in cleanroom environments and may need to follow Good Manufacturing Practices (GMP) and safety training. Their role ensures efficient and compliant production processes in pharmaceutical facilities.

What are some common challenges faced by Pharmaceutical Production Associates, and how can they be managed?

Pharmaceutical Production Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), meeting tight production schedules, and ensuring consistent product quality. Managing these challenges requires strong attention to detail, effective communication with team members, and a commitment to following standard operating procedures. Frequent training and collaboration with quality assurance teams can help associates stay updated on regulatory requirements and minimize errors, contributing to a smooth and efficient production process.

What is the role of a Production Associate?

A Pharmaceutical Production Associate is responsible for assembling, processing, and packaging medications in a manufacturing environment. They follow strict safety and quality protocols, operate production equipment, and document their work to ensure compliance with regulatory standards. Attention to detail and adherence to Good Manufacturing Practices (GMP) are essential in this role.

What is the difference between Pharmaceutical Production Associate vs Pharmaceutical Manufacturing Technician?

AspectPharmaceutical Production AssociatePharmaceutical Manufacturing Technician
CredentialsHigh school diploma or equivalent; GMP trainingHigh school diploma or equivalent; GMP training
Work EnvironmentCleanroom, manufacturing floors, lab settingsManufacturing floors, cleanrooms, labs
Job ResponsibilitiesAssisting in production, quality checks, equipment setupOperating machinery, maintaining production lines, quality control
Industry UsageCommonly used in pharmaceutical companies for entry-level rolesOften used interchangeably, but slightly more technical

The Pharmaceutical Production Associate and Pharmaceutical Manufacturing Technician roles share similar credentials and work environments, focusing on supporting pharmaceutical manufacturing processes. While both roles involve quality checks and equipment handling, the Technician may have more technical responsibilities like operating machinery. Both positions are essential in pharmaceutical production and often overlap in daily tasks, making them closely related in the industry.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Production Associate, and why are they important?

To thrive as a Pharmaceutical Production Associate, you need a solid understanding of Good Manufacturing Practices (GMP), attention to detail, and typically a high school diploma or relevant technical certification. Familiarity with automated production equipment, batch record systems, and basic laboratory tools is commonly required. Reliability, teamwork, and strong communication skills help ensure efficient operations and compliance with safety protocols. These skills and qualities are crucial for maintaining product quality, safety, and regulatory compliance in a highly regulated manufacturing environment.
What cities are hiring for Pharmaceutical Production Associate jobs? Cities with the most Pharmaceutical Production Associate job openings:
What are the most commonly searched types of Pharmaceutical Production jobs? The most popular types of Pharmaceutical Production jobs are:
What states have the most Pharmaceutical Production Associate jobs? States with the most job openings for Pharmaceutical Production Associate jobs include:

Associate Director, Drug Product Development

Jazz Pharmaceutical

Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago


Job description

If you are a current Jazz employee please apply via the Internal Career site
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.
Job Description
The Associate Director of Drug Product Development is responsible for providing scientific and technical leadership for Jazz Pharmaceuticals' Pharmaceutical Development programs at various stages of the development life-cycle including preformulation, formulation and process development, technical transfer and validation. The Associate Director of Drug Product Development will oversee drug product aspects of development and manufacturing projects from pre-formulation and product feasibility through to clinical trial supply and technology transfer/commercialization. In addition, the Associate Director of Drug Product Development may provide leadership of cross-functional CMC development teams. The Associate Director of Drug Product Development will have broad experience in pharmaceutical product development, demonstrated problem solving ability, module 3 authorship, development of robust manufacturing processes through designed experiments and data analysis, and excellent project management, teamwork and leadership skills.
Essential Functions
  • Leads the development of small molecule drug product formulations, appropriate to the phase of pharmaceutical development, with sufficient stability and robustness for clinical and/or commercial manufacturing.
  • Responsible for specifying product and process requirements, including manufacturing equipment and methods, performance criteria, materials, test protocols, required analytical methodology, packaging (clinical and commercial); and in developing robust processes for pharmaceutical production.
  • Directs projects and leads cross-functional teams (as required) with technical proficiency, scientific creativity, collaboration with others to achieve project goals on time and within budget.
  • Create intellectual property covering Jazz Pharmaceuticals products and ensure freedom to operate in the development of new drug products
  • Support the identification and selection of suitable drug product development and commercial manufacturing vendors (CMOs).
  • Direct technical projects (internally and at CDMOs) including developing detailed technical work plans and managing performance of vendors.
  • Work cooperatively with, or lead, internal and external teams as required.
  • Author CMC sections of regulatory dossiers for products at all stages to enable acceptance by global regulators.
  • Supports asset due diligence and new product introduction and integrations
  • Apply current knowledge of cGMP and industry standards for process design and validation to manage vendors and contract development organizations.

Required Knowledge, Skills, and Abilities
  • >10 years' experience in drug product development in the pharmaceutical industry required. Direct experience with formulation development, process development, technical transfer and/or process validation.
  • Demonstrated technical proficiency, engineering, collaboration with others, and independent thought. Strong teamwork skills.
  • Demonstrated troubleshooting and problem-solving skills including the use of designed experiments, statistical process control,
  • Development/authorship of CMC regulatory filings for pharmaceutical products.
  • Broad exposure to multiple drug delivery technologies and knowledge of standard dosage forms preferred.
  • Excellent written and verbal communication skills
  • Current knowledge of quality systems and FDA and EU regulations as they relate to pharmaceutical development and validation.
  • Experience in intellectual property development desirable.
  • Proven project management skills for technical programs.
  • Flexibility to travel on company business when required

Required/Preferred Education and Licenses
  • Advanced degree in Chemistry, Pharm. Sci., Engineering, or related field, or equivalent combination of education and work-related experience required.

Description of Physical Demands
  • Occasional mobility within office environment. Routinely sitting for extended periods of time.
  • Constantly operating a computer, printer, telephone and other similar office machinery.

Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.
FOR US BASED CANDIDATES ONLY
Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is:
$157,600.00 - $236,400.00
Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.
At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.
The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html