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Api Pharmaceutical Jobs (NOW HIRING)

Acuren Inspection, Inc.

API 510/570 Inspector

Torrance, CA · On-site

$37.50 - $60.58/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Position Summary Acuren is currently recruiting for an API 510/570 Inspector. Responsibilities * At ... pharmaceutical, aerospace and automotive industries. Acuren employs over 4,000 dedicated ...

Acuren Inspection, Inc.

API 510/570 Inspector

Torrance, CA · On-site +1

$37.50 - $60.58/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Position Summary Acuren is currently recruiting for an API 510/570 Inspector. Responsibilities * At ... pharmaceutical, aerospace and automotive industries. Acuren employs over 4,000 dedicated ...

Acuren Inspection, Inc.

API 510/570 Inspector

Torrance, CA

$37.50 - $60.58/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Acuren is currently recruiting for an API 510/570 Inspector. * At the direction of client, perform ... pharmaceutical, aerospace and automotive industries. Acuren employs over 4,000 dedicated ...

Merck & Co., Inc.

Director, Operations - API

Elkton, VA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience in small molecule API manufacturing or commercial pharmaceutical operations. * Prior ... experience supporting a manufacturing site start-up, transformation, or ramp-up. * Experience ...

Merck

Director, Operations - API

Elkton, VA

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Director, IPT Leader, API provides leadership, technical and operational expertise to the ... molecule pharmaceutical manufacturing facility, including project and site readiness ...

MSD

Director, Operations - API

Elkton, VA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience in small molecule API manufacturing or commercial pharmaceutical operations. * Prior ... experience supporting a manufacturing site start-up, transformation, or ramp-up. * Experience ...

MSD Malaysia

Director, Operations - API

Virginia, MN · On-site

$173.20 - $272.60/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience in small molecule API manufacturing or commercial pharmaceutical operations.* Prior ... experience supporting a manufacturing site start-up, transformation, or ramp-up.* Experience ...

Merck & Co.

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience in small molecule API manufacturing or commercial pharmaceutical operations. Prior ... experience supporting a manufacturing site start-up, transformation, or ramp-up. Experience ...

Merck & Co.

Director, Operations - API

Elkton, VA · On-site

$173.20 - $272.60/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience in small molecule API manufacturing or commercial pharmaceutical operations. * Prior ... experience supporting a manufacturing site start-up, transformation, or ramp-up. * Experience ...

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Api Pharmaceutical information

What is an API Pharmaceutical?

An API (Active Pharmaceutical Ingredient) Pharmaceutical job involves the research, development, production, and quality control of active ingredients used in medications. Professionals in this field work in manufacturing facilities or laboratories, ensuring that APIs meet regulatory standards and are produced efficiently. Roles can include chemists, process engineers, quality assurance specialists, and regulatory professionals. These jobs are essential in the pharmaceutical industry as APIs are the key components that provide therapeutic effects in medicines.

What are some typical challenges faced in an API Pharmaceutical role?

Professionals working in API Pharmaceutical roles often encounter challenges such as maintaining strict compliance with regulatory standards and navigating complex production processes. Meeting batch quality requirements and addressing potential deviations or equipment failures requires a proactive mindset and meticulous record-keeping. Additionally, coordinating closely with quality assurance and cross-functional teams is essential to ensure seamless operations and timely problem resolution. Overcoming these challenges helps ensure safe, effective, and high-quality API production, which is critical to the broader pharmaceutical supply chain.

What are the key skills and qualifications needed to thrive in the API Pharmaceutical position, and why are they important?

To thrive in an API Pharmaceutical role, you need a solid background in chemistry, process engineering, and pharmaceutical manufacturing regulations, often supported by a degree in pharmacy, chemistry, or chemical engineering. Experience with laboratory instruments, GMP/GLP compliance, and knowledge of quality management systems or regulatory documentation is highly valued. Effective problem-solving, teamwork, and attention to detail help professionals excel in fast-paced production and development environments. These skills are crucial for ensuring safe, efficient, and compliant production of Active Pharmaceutical Ingredients (APIs) essential to the healthcare industry.

More about Api Pharmaceutical jobs

What are the most commonly searched types of Api Pharmaceutical jobs?

The most popular types of Api Pharmaceutical jobs are:

What states have the most Api Pharmaceutical jobs?

States with the most job openings for Api Pharmaceutical jobs include:

What job categories do people searching Api Pharmaceutical jobs look for?

The top searched job categories for Api Pharmaceutical jobs are:

Api Pharmaceutical jobs near you
Infographic showing various Api Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Quality Assurance Training Specialist II

Merck Group

Saint Louis, MO • On-site

$70K - $111K/yr

Full-time

Medical, Retirement, PTO

Re-posted 15 days ago

Job description

Work Your Magic with us! Start your next chapter and join MilliporeSigma.
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
At MilliporeSigma, as the Quality Assurance Training Specialist 2 at our St. Louis Cherokee CDMO facility, you will be expected to design, develop, facilitate and lead site/staff training programs and initiatives while fostering a collaborative learning culture. You will implement and direct the site training program and oversee training performance and compliance across all site departments. You will be responsible for management of the site training program, including management of the training curriculums and continuous improvement of the training systems to ensure they remain consistent with current expectations for cGMP training programs. This position requires knowledge and understanding of cGMP guidelines as they pertain to training requirements within the API pharmaceutical manufacturing industry, including quality regulations, training development and delivery, and change management.
The ideal candidate will have a passion for success enabled through training and development of employees through administration of programs that will improve skills and knowledge. The candidate will showcase initiative in identifying and implementing improvement projects to influence change in training programs and strengthen system compliance.
This position will be responsible for:
  • Definition, implementation, and oversight of the site training program for all departments, including the process and requirements for training curriculums and learning items.
  • Leading the cross-functional site Training Review Board to ensure proactive discussion and alignment of site training requirements across all site roles.
  • Development, maintenance, and organization of training curriculums and learning materials for site wide programs, including but not limited to, New Employee Onboarding, cGMP/GDP, and Data Integrity, and Train the Trainer.
  • Delivery of classroom and on-the-job training associated with quality events and/or cGMP requirements.
  • Management of training requirements, assignments, and completions in the electronic Learning Management System (LMS)
  • Writing and revising QA operating procedures, work instructions, forms, and job aids related to the training program with minimal supervision
  • Creation and tracking of key performance indicators demonstrating successful training compliance.
  • Act as Subject Matter Expert for the site training program in internal, customer, and regulatory audits.
  • Travel-up to 5%

Who You Are
Minimum Qualifications:
  • Bachelor's degree in any discipline
  • 5+ years' experience working in a quality role within a cGMP regulated pharmaceutical environment
  • 2+ years' experience in a training role or function

Preferred Qualifications:
  • Strong working knowledge of cGMP and regulatory standards as they pertain to Quality Systems and Training
  • Independent, self-starter with proven results in training environment
  • Experience working with Training systems to track and evaluate compliance management and program effectiveness.
  • Strong interpersonal and communication skills.
  • Ability to lead discussions and instruct participants in training classes using a variety of instructional techniques.
  • Strong teaching and facilitation skills.
  • Ability to work and communicate well with other key groups to achieve improvement and operational results.
  • Demonstrated knowledge and experience in various computer skills, including Windows, Word for Windows, Excel, and Outlook, as well as familiarity working in a window-based environment.
  • Demonstrated experience in detailed review work and following procedures, especially in a GMP regulated industry.

Pay Range for this position: $70,600-$111,000 per year
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Apply