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Api Manufacturing Jobs (NOW HIRING)

TekWissen LLC

Manufacturing Associate

Portsmouth, NH · On-site

$20 - $26/hr

Manufacture therapeutic proteins (API) in accordance with cGMP requirements. * Execute process recipes and follow established SOPs and batch records. * Set up, operate, and monitor manufacturing ...

Merck & Co.

Senior Scientist, Chemistry

Rahway, NJ

$92K - $126K/yr

The role is tasked with solving high complexity analytical problems related to the development and validation of API manufacturing processes for the commercialization of our Company innovative drug ...

MSD

Director, Operations - API

Elkton, VA

Join a purpose-built, agile small molecule manufacturing site where your work will help bring ... The Director, IPT Leader, API provides leadership, technical and operational expertise to the ...

Stark Pharma Solutions Inc

Senior Process Engineer

Bend, OR · On-site

$109K - $141K/yr

Bend, OR Duration: 12+ Month Contract Position Overview We are seeking an experienced Senior Process Engineer to support pharmaceutical and API manufacturing projects from design through ...

Merck

Director, Operations - API

Elkton, VA

Join a purpose-built, agile small molecule manufacturing site where your work will help bring ... The Director, IPT Leader, API provides leadership, technical and operational expertise to the ...

MSD

Senior Scientist, Chemistry

Rahway, NJ

$92K - $126K/yr

The role is tasked with solving high complexity analytical problems related to the development and validation of API manufacturing processes for the commercialization of our Company innovative drug ...

Merck & Co.

Director, Operations - API

Elkton, VA · On-site

$173.20 - $272.60/hr

Join a purpose-built, agile small molecule manufacturing site where your work will help bring ... Lead the development of the future-state operating model for the API operations at Elkton, VA.

Merck & Co.

Join a purpose-built, agile small molecule manufacturing site where your work will help bring ... The Director, IPT Leader, API provides leadership, technical and operational expertise to the ...

MSD Malaysia

Director, Operations - API

Virginia, MN · On-site

$173.20 - $272.60/hr

Join a purpose-built, agile small molecule manufacturing site where your work will help bring ... The Director, IPT Leader, API provides leadership, technical and operational expertise to the ...

New

Merck & Co., Inc.

Senior Scientist, Chemistry

Rahway, NJ · On-site

$92K - $126K/yr

The role is tasked with solving high complexity analytical problems related to the development and validation of API manufacturing processes for the commercialization of our Company innovative drug ...

BoehringerPRD

In-depth expertise in pharmaceutical analysis, quality assurance, and API manufacturing operations. * Extensive experience in cross-functional and cross-country collaboration and proven ability to ...

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Showing results 41-60

All JobsApi Manufacturing Jobs

Api Manufacturing information

See salary details

$30.5K

$97.6K

$153.5K

How much do api manufacturing jobs pay per year?

As of Aug 8, 2026, the average yearly pay for api manufacturing in the United States is $97,556.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,000.00 and $120,500.00 per year, depending on experience, location, and employer.

What kinds of teams or departments do api manufacturing professionals typically collaborate with?

API Manufacturing professionals often work closely with quality assurance, process development, engineering, and regulatory affairs teams to ensure safe and compliant production of pharmaceutical ingredients. Daily responsibilities may involve coordinating with maintenance staff for equipment upkeep and troubleshooting, as well as working with quality control analysts to monitor product specifications. This collaborative environment fosters continuous improvement and adherence to strict industry standards, making strong communication and teamwork vital. Joining an API manufacturing team often provides exposure to cross-functional projects and potential pathways for advancement into supervisory or technical specialist roles.

What are the key skills and qualifications needed to thrive in api manufacturing?

To thrive in API Manufacturing, you need a solid understanding of chemical processes, current Good Manufacturing Practices (cGMP), and safety regulations, typically supported by a degree in chemistry, chemical engineering, or a related field. Experience with process control systems, laboratory information management systems (LIMS), and relevant safety certifications such as OSHA are essential. Strong attention to detail, teamwork, and problem-solving skills are valued soft skills in this setting. These capabilities ensure production efficiency, regulatory compliance, and safety in the manufacture of active pharmaceutical ingredients.

What is an api manufacturing?

An API Manufacturing job involves the production of Active Pharmaceutical Ingredients (APIs), which are the key components in medications. Professionals in this field oversee chemical synthesis, purification, and quality control processes to ensure that APIs meet regulatory and safety standards. They work in pharmaceutical manufacturing facilities, following strict guidelines set by regulatory bodies like the FDA and EMA. The role often includes maintaining Good Manufacturing Practices (GMP), troubleshooting production issues, and optimizing processes for efficiency and quality.

More about Api Manufacturing jobs
What are the most commonly searched types of Api Manufacturing jobs? The most popular types of Api Manufacturing jobs are:
What states have the most Api Manufacturing jobs? States with the most job openings for Api Manufacturing jobs include:
What job categories do people searching Api Manufacturing jobs look for? The top searched job categories for Api Manufacturing jobs are:
Api Manufacturing jobs near you
Infographic showing various Api Manufacturing job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 4% Part Time, 1% Temporary, 4% Contract, and 3% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $97,556 per year, or $46.9 per hour.

Project Manager, Peptide API Operations

Hims and Hers Health, Inc.

Menlo Park, CA • On-site

$110K - $130K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 days ago

Job description

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we're making better health outcomes easier to achieve.
Hims & Hers is a public company, traded on the NYSE under the ticker symbol "HIMS." To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company's outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals.
About the Role:
We are seeking a highly organized and execution-focused Project Manager to lead ramp-up and tech transfer activities for a peptide API manufacturing facility. This role will drive cross-functional coordination across Operations, Quality (QA/QC), and global partners to ensure successful process transfer, facility readiness, and on-time program delivery. The ideal candidate thrives in a fast-paced ramp-up environment and can manage complexity while keeping teams aligned and accountable.
You Will:
  • Lead end-to-end project management for peptide manufacturing technology transfers, process implementation, and startup activities.
  • Develop, maintain, and execute detailed project plans, timelines, milestones, and risk mitigation strategies across multiple programs.
  • Coordinate the transfer of peptide manufacturing processes, including SPPS, purification, and lyophilization, from R&D or external manufacturing sites into commercial operations.
  • Partner with Manufacturing, Engineering, Quality, and Process Development teams to ensure successful process validation and GMP manufacturing readiness.
  • Serve as the primary cross-functional project lead, coordinating activities across Operations, QA/QC, Engineering, Supply Chain, and global stakeholders.
  • Facilitate project meetings, drive accountability, resolve cross-functional issues, and communicate project status to leadership.
  • Partner with Quality to ensure all project activities comply with cGMP requirements and support the development of SOPs, batch records, validation protocols, and other controlled documentation.
  • Support facility startup activities, including equipment qualification (IQ/OQ/PQ), operational readiness, and execution of initial GMP manufacturing campaigns.
  • Help establish scalable project management processes, governance, and best practices to support a growing manufacturing organization.
  • Collaborate with global teams and external partners to align technical requirements, project timelines, and key deliverables while effectively managing communication across multiple time zones.

You Have:
  • Bachelor's degree in Chemical Engineering, Chemistry, Life Sciences, or a related scientific discipline.
  • 5+ years of project management experience in pharmaceutical, biotechnology, or other regulated manufacturing environments.
  • Direct experience leading technology transfer, process scale-up, manufacturing startup, or commercialization projects strongly preferred.
  • Experience supporting peptide API manufacturing or other complex chemical manufacturing processes is a plus.
  • Demonstrated success managing complex, cross-functional projects with aggressive timelines and multiple stakeholders.
  • Strong understanding of technology transfer, process validation, and cGMP manufacturing workflows.
  • Proven ability to influence cross-functional teams and drive alignment without direct authority.
  • Highly organized with the ability to balance structure and execution in a fast-paced, evolving environment.
  • Strong risk management and problem-solving skills, with the ability to anticipate challenges and implement practical solutions.
  • Excellent written and verbal communication skills, with experience presenting to both technical and non-technical stakeholders.
  • Comfortable collaborating with global teams and working flexible hours as needed to support international partners and project milestones.

Our Benefits (there are more but here are some highlights):
  • Competitive salary & equity compensation for full-time roles
  • Unlimited PTO, company holidays, and quarterly mental health days
  • Comprehensive health benefits including medical, dental & vision, and parental leave
  • Employee Stock Purchase Program (ESPP)
  • 401k benefits with employer matching contribution
  • Offsite team retreats

We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply-even if you're not sure if your background or experience is a perfect match.
Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@forhims.com and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address.
To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.

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