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Contract Manufacturing Specialist Jobs (NOW HIRING)

Tekberry

Manufacturing Specialist

Colorado Springs, CO · On-site

$35/hr

Contract, 2 years Shift Schedule: Day Shift, Monday-Friday Location: Colorado Springs, CO Job Code: JPC-12484 Tekberry is looking for a highly qualified and motivated Manufacturing Specialist to work ...

TEKBERRY

Manufacturing Specialist

Colorado Springs, CO · On-site

$35/hr

Contract, 2 years Shift Schedule: Day Shift, Monday-Friday Location: Colorado Springs, CO Job Code: JPC-12484 Tekberry is looking for a highly qualified and motivated Manufacturing Specialist to work ...

SpectronRx

Manufacturing Specialist

South Bend, IN · On-site

$28 - $35/hr

COMPANY OVERVIEW SpectronRx is a rapidly growing Contract Development and Manufacturing ... We are seeking an experienced Manufacturing Specialist to join our growing company. The ...

Siemens

Head of Contract Manufacturing

Kenosha, WI · On-site

$145K - $248K/yr

Head of Contract Manufacturing SI EA US Here at Siemens, we take pride in enabling sustainable ... In this role you will lead a team of specialists and leaders that will oversee the day-to-day ...

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Contract Manufacturing Specialist information

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$13

$28

$48

How much do contract manufacturing specialist jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for contract manufacturing specialist in the United States is $28.04, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $36.30 per hour, depending on experience, location, and employer.

What does a contract manufacturing specialist do?

A Contract Manufacturing Specialist manages relationships and processes between a company and its third-party manufacturers. They are responsible for coordinating production schedules, ensuring quality standards are met, and negotiating contracts with manufacturing partners. Their role also includes monitoring compliance with regulations, troubleshooting production issues, and optimizing supply chain efficiency. Overall, they help ensure that products are manufactured cost-effectively and delivered on time.

What skills and qualifications are needed to be a contract manufacturing specialist?

To thrive as a Contract Manufacturing Specialist, you need a solid understanding of supply chain management, contract negotiation, and quality assurance, often supported by a degree in engineering, business, or a related field. Familiarity with ERP systems, quality management software, and relevant certifications like Six Sigma or APICS can be highly beneficial. Strong project management, problem-solving abilities, and effective communication are critical soft skills for coordinating with vendors and internal teams. These skills ensure efficient production processes, compliance with standards, and successful partnerships with manufacturing contractors.

What is the difference between Contract Manufacturing Specialist vs Quality Control Specialist?

AspectContract Manufacturing SpecialistQuality Control Specialist
CredentialsRelevant technical certifications, industry-specific trainingQuality assurance certifications, such as CQE or Six Sigma
Work EnvironmentManufacturing plants, production facilitiesLaboratories, inspection sites
Employer & Industry UsageManufacturing companies across various sectorsQuality assurance departments in manufacturing and pharma

While both roles are vital in manufacturing, a Contract Manufacturing Specialist focuses on managing production processes and supplier relationships, whereas a Quality Control Specialist ensures products meet quality standards. Understanding these differences helps in selecting the right career path or job focus within manufacturing industries.

How does a contract manufacturing specialist collaborate with internal teams and external partners?

A Contract Manufacturing Specialist works closely with internal departments such as procurement, quality assurance, and supply chain to ensure that all manufacturing processes meet company standards and timelines. Externally, they liaise with third-party manufacturers to negotiate contracts, monitor production schedules, and address any issues that arise. Effective communication and project management skills are vital, as the specialist is often the main point of contact between the organization and its manufacturing partners. This collaboration ensures that products are delivered on time, within budget, and according to quality requirements.
More about Contract Manufacturing Specialist jobs
What cities are hiring for Contract Manufacturing Specialist jobs? Cities with the most Contract Manufacturing Specialist job openings:
What states have the most Contract Manufacturing Specialist jobs? States with the most job openings for Contract Manufacturing Specialist jobs include:
What job categories do people searching Contract Manufacturing Specialist jobs look for? The top searched job categories for Contract Manufacturing Specialist jobs are:
Contract Manufacturing Specialist jobs near you
Infographic showing various Contract Manufacturing Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $58,318 per year, or $28 per hour.

Principal External Manufacturing Specialist (Drug Product)

Regeneron Pharmaceuticals, Inc.

Rensselaer, NY • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 19 days ago

Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical

Job description

Build our future together:
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking to fill multiple External Manufacturing Specialist positions at the Principal or Senior level. The Senior/Principal External Manufacturing Specialist oversees all aspects of external manufacturing contract manufacturing operations (filling, assembly, packaging) including day-to-day operations, ensuring timely completion of associated operations/documentation and assisting in the monitoring of cGMP compliance. Additionally, the role provides guidance to other specialists as well as consults with management on all contract manufacturing operations and GMP compliance issues.
When & where:
  • Location: East Greenbush, New York, United States
  • Work model: Monday-Friday, 8am-4:30pm
  • Travel: up to 25%

Discover your role:
  • Serves as a Regeneron operational contact for contract manufacturing and/or business partner sites concerning day-to-day activities.
  • Coordinates external manufacturing activities at contract and/or business partner sites, including but not limited to: scheduling of all batches, supply of materials, providing direction on shipment of bulk or finished product, tracking and monitoring of cycle times, providing supporting documentation for manufacturing activities and enlisting support from others who will provide any required associated reports and technical expertise.
  • Coordinates/oversees multiple external manufacturing activities at multiple sites, as required.
  • Liaises between various departments within Regeneron including, but not limited to Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments, Legal, Regulatory, Strategic Sourcing and contract manufacturers or business partners.
  • Leads sub-teams in continuous process improvements, system/equipment implementation and/or strategy development.
  • Leads or supports all investigations which concern external manufacturing and associated shipping operations.
  • Ensures product integrity and company reputation monitoring of cGMP compliance at external manufacturing contract manufacturers and business partners.
  • Performs reviews of pre-production master batch records and executed batch records.
  • Authors documents and procedures.
  • Supports audit operations, both internal and external.
  • Analyzes data for trends and potential issues.
  • Travels 25% (target) or more (domestic and international), as required.

This role requires:
  • BS/BA in a scientific discipline and the following years of experience in cGMP manufacturing operations (clinical and/or commercial external manufacturing), including experience collaborating with CMOs/CROs, or equivalent combination of education and experience, for each level:
    • Senior Specialist - 5+ years
    • Principal Specialist - 8+ years
    • Level will be determined based on experience
  • Knowledge of external manufacturing from formulation through the final package.
  • Knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations.
  • Proficient in Excel, PowerPoint, Visio, Word, Oracle etc. in addition to experience working within shared work environments.
  • Strong interpersonal, written and oral communication skills.
  • Confidence, has a high emotional IQ, and has strong interpersonal, written and oral communication skills for providing team updates.
  • Ability to impart understanding of provided instructions, develop instructions and sets and works towards goals with minimal supervision.
  • A degree of ingenuity, creativity and resourcefulness in evolving and ambiguous environments.
  • Resiliency and flexibility in the face of challenges and adversarial situations.
  • Understanding and listening to team members and stakeholders needs while supporting productive team environments toward a common objective.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about on-site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$78,700.00 - $150,600.00

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