ZipRecruiter

Log In

1

Pharmaceutical Manufacturing Analyst Jobs (NOW HIRING)

kindeva

Manufacturing Engineer

Maryland Heights, MO · On-site

$70K - $90K/yr

... pharmaceutical regulatory requirements. * Strong analytical and problem-solving skills ... Knowledge of Lean Manufacturing or Six Sigma principles. * Familiarity with automated inspection ...

kindeva

Manufacturing Engineer

Maryland Heights, MO · On-site

$70K - $90K/yr

... pharmaceutical regulatory requirements. * Strong analytical and problem-solving skills ... Knowledge of Lean Manufacturing or Six Sigma principles. * Familiarity with automated inspection ...

kindeva

Manufacturing Engineer

Maryland Heights, MO · On-site

$70K - $90K/yr

... pharmaceutical regulatory requirements. * Strong analytical and problem-solving skills ... Knowledge of Lean Manufacturing or Six Sigma principles. * Familiarity with automated inspection ...

kindeva

Manufacturing Engineer

Maryland Heights, MO · On-site

$70K - $90K/yr

... pharmaceutical regulatory requirements. * Strong analytical and problem-solving skills ... Knowledge of Lean Manufacturing or Six Sigma principles. * Familiarity with automated inspection ...

previous page

Showing results 41-60

All JobsHealthcare JobsMedical Specialists JobsClinical Pharmacist JobsPharmaceutical Manufacturing Analyst Jobs

Pharmaceutical Manufacturing Analyst information

See salary details

$30.5K

$73.6K

$113.5K

How much do pharmaceutical manufacturing analyst jobs pay per year?

As of Sep 10, 2026, the average yearly pay for pharmaceutical manufacturing analyst in the United States is $73,632.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,000.00 and $95,000.00 per year, depending on experience, location, and employer.

What is a pharmaceutical manufacturing analyst?

Pharmaceutical Manufacturing Analysts are professionals responsible for testing, analyzing, and ensuring the quality of pharmaceutical products during the manufacturing process. They perform laboratory tests, validate manufacturing procedures, and monitor compliance with industry regulations such as Good Manufacturing Practices (GMP). Their work helps ensure that medications are safe, effective, and meet quality standards before reaching consumers.

What are the key skills and qualifications needed to thrive as a pharmaceutical manufacturing analyst?

To thrive as a Pharmaceutical Manufacturing Analyst, you need strong analytical skills, knowledge of Good Manufacturing Practices (GMP), and a background in chemistry, biology, or a related scientific field, often supported by a relevant degree. Familiarity with laboratory equipment, quality control systems, and regulatory compliance tools such as LIMS (Laboratory Information Management Systems) is typically required. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for ensuring accuracy and collaboration. These skills are crucial for maintaining product quality, meeting regulatory standards, and ensuring the safety and efficacy of pharmaceutical products.

How does a pharmaceutical manufacturing analyst typically collaborate with other departments during the production process?

A Pharmaceutical Manufacturing Analyst works closely with quality assurance, production, and research and development teams to ensure products meet regulatory standards and company specifications. They regularly communicate analytical results, investigate deviations, and contribute to process improvements. Collaboration often involves participating in cross-functional meetings, supporting validation efforts, and ensuring timely release of materials, making teamwork and clear communication key aspects of the role.

What is the difference between Pharmaceutical Manufacturing Analyst vs Quality Control Analyst?

AspectPharmaceutical Manufacturing AnalystQuality Control Analyst
CredentialsBachelor's in Pharmacy, Chemistry, or related field; sometimes certifications in GMPBachelor's in Chemistry, Biology, or related; certifications in GMP or QC preferred
Work EnvironmentManufacturing facilities, production lines, labsLaboratories, testing facilities, quality assurance departments
Employer & Industry UsagePharmaceutical manufacturing companies, biotech firmsPharmaceutical companies, contract labs, biotech firms
Common Search & ComparisonYesYes

While both roles support pharmaceutical production, a Pharmaceutical Manufacturing Analyst focuses on analyzing manufacturing processes and optimizing production efficiency, whereas a Quality Control Analyst primarily tests and inspects products to ensure quality standards are met. Both roles require knowledge of GMP and work within the pharmaceutical industry, but their daily tasks and focus areas differ.

Is pharmaceutical manufacturing a good job?

Pharmaceutical manufacturing analysts play a key role in ensuring the quality and compliance of drug production processes. The job typically involves working in controlled environments, using specialized equipment, and requires attention to detail and knowledge of Good Manufacturing Practices (GMP). It can offer stable employment with opportunities for advancement in the healthcare and biotech industries.

What are popular job titles related to Pharmaceutical Manufacturing Analyst jobs?

For Pharmaceutical Manufacturing Analyst jobs, the most frequently searched job titles are:

Infographic showing various Pharmaceutical Manufacturing Analyst job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 4% Part Time, 3% Contract, and 3% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $73,632 per year, or $35.4 per hour.

Manufacturing Pharmaceutical Technician

Wilson, NC • On-site

The Rockridge Group
See more jobs at The Rockridge Groupexternal

Full-time

Re-posted 6 days ago

Key responsibilities

  • Follow Master Batch Records to manufacture controlled, oral solid dose (OSD) and other dosage forms.

  • Set up, operate, and clean manufacturing equipment while adhering to SOPs and regulatory guidelines.

  • Perform in-process testing and inspections, and document data accurately and timely.

Job description

TITLE:  Manufacturing Pharmaceutical Technician 
LOCATION: Wilson, NC (onsite)
DURATION: 6-12 months (7/7/25-7/6/26)
SHIFT:  Monday thru Thursday 
TIME:  4:00PM-2:30AM
 
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.
  • The Pharmaceutical Technician has no direct reports.
 
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.
 
 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.