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Parenteral Manufacturing Jobs (NOW HIRING)

Experience supporting sterile, aseptic, biologics, or parenteral manufacturing operations. * Knowledge of CAPA, Change Control, Risk Assessments, and Quality Management Systems. * Lean, Six Sigma, or ...

$111K - $202K/yr

The Associate Director of Business Development in Parenteral Drug Delivery is responsible for ... Experience with CDMO or contract manufacturing * Knowledge of drug delivery systems and solutions

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Parenteral Manufacturing information

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$30K

$69.5K

$121K

How much do parenteral manufacturing jobs pay per year?

As of Sep 7, 2026, the average yearly pay for parenteral manufacturing in the United States is $69,454.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,000.00 and $83,000.00 per year, depending on experience, location, and employer.

What is parenteral manufacturing?

Parenteral manufacturing is the process of producing sterile pharmaceutical products that are administered by injection through routes such as intravenous, intramuscular, or subcutaneous methods. This process requires strict aseptic techniques and highly controlled environments to prevent contamination, as parenteral products bypass the body’s natural barriers. The manufacturing process includes compounding, filling, sealing, and sterilizing the products, often in the form of solutions, suspensions, or emulsions. Quality control and regulatory compliance are critical to ensure the safety and efficacy of these injectable medications.

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

To thrive in Parenteral Manufacturing, you need a solid understanding of sterile manufacturing processes, Good Manufacturing Practices (GMP), and often a background in pharmacy, chemistry, or life sciences. Familiarity with aseptic processing equipment, cleanroom protocols, and regulatory compliance systems such as FDA or EMA guidelines is typically required. Attention to detail, problem-solving abilities, and effective teamwork are crucial soft skills in this environment. These qualifications are essential to ensure product safety, regulatory compliance, and the consistent delivery of high-quality sterile pharmaceuticals.

What are some common challenges faced in parenteral manufacturing, and how can new employees effectively address them?

One common challenge in parenteral manufacturing is maintaining strict sterility throughout production, as even minor lapses can compromise product safety. New employees must become proficient in aseptic techniques and follow rigorous standard operating procedures to prevent contamination. Additionally, working in cleanroom environments requires attention to detail and adaptability to changing protocols as regulatory standards evolve. Collaborating closely with quality assurance and maintenance teams is essential for resolving issues quickly and ensuring compliance.

What is the difference between Parenteral Manufacturing vs Parenteral Quality Control?

AspectParenteral ManufacturingParenteral Quality Control
Primary RoleProducing sterile injectable productsTesting and ensuring product quality and safety
Required CredentialsPharmacy, pharmaceutical technology, or related certificationsQuality assurance, microbiology, or related certifications
Work EnvironmentManufacturing plants, sterile environmentsLaboratories, quality testing facilities
Industry UsagePharmaceutical manufacturing companiesQuality control labs within pharma companies

Parenteral Manufacturing focuses on producing sterile injectable drugs, while Parenteral Quality Control ensures these products meet safety and quality standards through testing. Both roles require related certifications and work within the pharmaceutical industry, but their core functions differ: manufacturing vs quality assurance.

What states have the most Parenteral Manufacturing jobs?

States with the most job openings for Parenteral Manufacturing jobs include:

What job categories do people searching Parenteral Manufacturing jobs look for?

The top searched job categories for Parenteral Manufacturing jobs are:

Infographic showing various Parenteral Manufacturing job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 4% Part Time, 3% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $69,454 per year, or $33.4 per hour.

Sr. Quality Assurance Specialist - 12-Hr Night Shift 2-2-3

Alcami Corporation

Morrisville, NC • On-site

$77K - $106K/yr

Full-time

Posted 3 days ago

New


Alcami rating

7.8

Company rating: 7.8 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

 

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team?

Job Summary

The Senior Quality Assurance Specialist is accountable for driving results in a fast-paced environment by effectively performing activities as directed to ensure quality and compliance with applicable regulatory requirements and internal procedures. These activities may include reviewing documents and data, conducting audits and inspections, hosting audits and inspections, and maintaining quality databases. The ideal candidate will assist internal teammates and partner with individuals from other departments for the development of SOPs and associated documents, and process improvements. The Sr. Quality Assurance Specialist will provide guidance and mentoring to Operations personnel in achieving a high level of GMP compliance and instilling quality culture.

On-Site Expectations
  • 100% on-site position.
  • Night Shift: 12-Hour Rotating (2-2-3), 7:00pm - 7:00am.
Responsibilities
  • Performs quality review and approval of documents, data, protocols, and/or reports.
  • Performs GMP document creation and issuance (batch records, logbooks, forms, etc.).
  • Performs visual inspection of parenteral product (requires qualification).
  • Performs internal quality audits and/or inspections.
  • Supports client audits and inspections, and regulatory inspections.
  • Maintains quality databases.
  • Assists with implementation and supports quality systems, including but not limited to, operations support, batch review and approval, training, vendor management, and overall regulatory inspectional readiness.
  • Assists with quality improvement initiatives as needed.
  • Consults with clients on production and documentation. 
  • Assists with development of SOPs or other quality documents.
  • Maintains accurate files and records.
  • Serves as an effective member of the Quality Assurance team and may serve as a mentor to others in area of expertise.
  • Complies with company polices and SOPs.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Other duties as assigned.
Qualifications
  • Bachelor's degree in Chemistry, Biology, or related field with 5-7+ years of GMP related experience, or Master's degree in related field. 
Knowledge, Skills, and Abilities
  • Aseptic parenteral manufacturing.
  • Grade C gowning.
  • GMP and Annex 1 experience.
  • 20/20 corrected vision for Visual Inspector qualification.
Travel Expectations
  • Rarely may be requested to travel to support other Alcami sites.
Physical Demands and Work Environment

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to stand. The employee is occasionally required to walk; sit and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.

While performing the duties of this job, the employee is frequently exposed to moving mechanical parts and the risk of electrical shock, burn hazards and microbial contamination. The employee is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc.

Employment Type: FULL_TIME

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