Overview Overview A global biopharmaceutical company on a mission to Solve On, Incyte follows ... manufacturing, supply chain, engineering, and quality operations. The individual will partner ...
Overview Overview A global biopharmaceutical company on a mission to Solve On, Incyte follows ... manufacturing, supply chain, engineering, and quality operations. The individual will partner ...
CSL Plasma is a subsidiary of CSL, a global biopharma company. Plasma collected at CSL Plasma facilities is used by CSL for the sole purpose of manufacturing lifesaving plasma-derived therapies for ...
CSL Plasma is a subsidiary of CSL, a global biopharma company. Plasma collected at CSL Plasma facilities is used by CSL for the sole purpose of manufacturing lifesaving plasma-derived therapies for ...
Biopharmaceutical Manufacturing Associate information
See Delaware salary details
$18.53 - $20.49
4% of jobs
$20.49 - $22.46
6% of jobs
$23.11 is the 25th percentile. Wages below this are outliers.
$22.46 - $24.43
44% of jobs
$24.43 - $26.40
9% of jobs
$26.40 - $28.37
3% of jobs
$28.37 - $30.34
1% of jobs
$31.16 is the 75th percentile. Wages above this are outliers.
$30.34 - $32.30
16% of jobs
$32.30 - $34.27
15% of jobs
$34.27 - $36.24
0% of jobs
$36.24 - $38.21
0% of jobs
$38.21 - $40.18
1% of jobs
$18
$27
$40
How much do biopharmaceutical manufacturing associate jobs pay per hour?
As of Aug 9, 2026, the average hourly pay for biopharmaceutical manufacturing associate in Delaware is $27.14, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.78 per hour, depending on experience, location, and employer.
What is the difference between Biopharmaceutical Manufacturing Associate vs Quality Control Technician?
| Aspect | Biopharmaceutical Manufacturing Associate | Quality Control Technician |
|---|---|---|
| Primary Role | Supports production processes, prepares materials, and ensures manufacturing runs smoothly | Performs testing and inspection of products to ensure quality standards |
| Required Skills | Knowledge of GMP, aseptic techniques, and manufacturing procedures | Laboratory skills, attention to detail, knowledge of testing methods |
| Work Environment | Cleanrooms, manufacturing floors, production facilities | Laboratories, testing labs, quality control areas |
| Certifications | GMP training, sometimes cGMP certification | Lab safety, GMP, and quality assurance training |
The Biopharmaceutical Manufacturing Associate focuses on supporting the production process in manufacturing environments, while the Quality Control Technician specializes in testing and verifying product quality. Both roles require GMP knowledge and work in regulated settings, but their daily tasks and skill sets differ significantly.
What are some common challenges faced by biopharmaceutical manufacturing associates, and how can they be addressed?
Biopharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP) and troubleshooting equipment malfunctions under tight production schedules. To address these challenges, associates are trained extensively on standard operating procedures and cross-functional communication to quickly resolve issues. Teamwork and attention to detail are essential, as the role frequently involves collaborating with quality assurance, engineering, and process development teams to ensure product safety and compliance. Continuous learning and proactive problem-solving are key to success in this dynamic environment.
What is a biopharmaceutical manufacturing associate?
As a biopharmaceutical manufacturing associate, your primary responsibilities are to prepare equipment and materials for the production of biopharmaceutical products. Your duties include moving the product, supplies, and inventory to support the manufacturing process and operating devices like autoclaves and washers. You monitor the production and operations, make adjustments to increase efficiency, and ensure that you are meeting all safety regulations. You work with downstream and upstream processes to control quality. You are also in charge of preparing reports and reviewing GMP documents to ensure compliance with laws and industry regulations.
What are the key skills and qualifications needed to thrive as a biopharmaceutical manufacturing associate?
To thrive as a Biopharmaceutical Manufacturing Associate, you need a solid background in life sciences or engineering, with knowledge of GMP (Good Manufacturing Practices) and often a relevant bachelor’s degree or associate’s certification. Familiarity with bioprocessing equipment, automation systems like SCADA, and quality control tools is essential. Attention to detail, teamwork, and strong communication skills are crucial soft skills for this role. These competencies ensure the safe, accurate, and compliant production of high-quality biopharmaceutical products.
What does a biopharmaceutical manufacturing associate do?
A Biopharmaceutical Manufacturing Associate is responsible for producing biopharmaceutical products such as vaccines, antibodies, or therapeutic proteins under strict regulatory guidelines. Their tasks typically include preparing equipment, monitoring production processes, maintaining sterile environments, and ensuring that all procedures adhere to Good Manufacturing Practices (GMP). They may also be involved in quality control, documentation, and troubleshooting equipment issues. This role is crucial for ensuring the safety, efficacy, and quality of biopharmaceutical products.
More about Biopharmaceutical Manufacturing Associate jobs
What are popular job titles related to Biopharmaceutical Manufacturing Associate jobs in Delaware? For Biopharmaceutical Manufacturing Associate jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Biopharmaceutical Manufacturing Associate jobs in Delaware look for? The top searched job categories for Biopharmaceutical Manufacturing Associate jobs in Delaware are:
What cities in Delaware are hiring for Biopharmaceutical Manufacturing Associate jobs? Cities in Delaware with the most Biopharmaceutical Manufacturing Associate job openings:
Full-time
Posted 25 days ago
Job description
Overview
Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity.
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
Position Summary
The Global Head of Strategic Sourcing, Technical Operations is responsible for supporting the development and execution of global sourcing strategies related to Global Technical Operations across the enterprise. This role oversees category management, supplier strategy, and cost optimization initiatives spanning manufacturing, supply chain, engineering, and quality operations.
The individual will partner closely with Technical Operations leadership, R&D, Quality, and Finance to ensure supply continuity, drive operational excellence, and enable innovation across a complex global supplier ecosystem.
Key Responsibilities
Strategic Leadership
Category Management
Supplier Relationship Management
Cross-Functional Collaboration
Risk & Compliance
Team Leadership (if Director level)
Qualifications
Education
Experience
Industry Expertise
Core Competencies
Key Performance Indicators (KPIs)
Working Environment
Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity.
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
Position Summary
The Global Head of Strategic Sourcing, Technical Operations is responsible for supporting the development and execution of global sourcing strategies related to Global Technical Operations across the enterprise. This role oversees category management, supplier strategy, and cost optimization initiatives spanning manufacturing, supply chain, engineering, and quality operations.
The individual will partner closely with Technical Operations leadership, R&D, Quality, and Finance to ensure supply continuity, drive operational excellence, and enable innovation across a complex global supplier ecosystem.
Key Responsibilities
Strategic Leadership
- Support the implementation of the sourcing strategies defined by Technical Operations (e.g., CMOs/CDMOs, API, excipients, packaging, direct materials, engineering services, MRO, capital equipment).
- Align procurement strategies with enterprise objectives, including cost efficiency, resilience, sustainability, and innovation.
- Act as a strategic advisor to Technical Operations leadership on supply market trends, risk mitigation, and supplier capabilities.
Category Management
- Lead and partner to build global category strategies including demand aggregation, supplier segmentation, and total cost of ownership optimization.
- Identify and deliver cost savings, cost avoidance, and value creation initiatives.
- Implement best-in-class procurement and sourcing practices, including RFx, should-cost modeling, long-term contracting, and periodic rate negotiations to ensure vendors remain cost-competitive within their respective markets.
Supplier Relationship Management
- Manage suppliers that deliver activities for more than one department.
- Leverage work contracted across multiple division of the same supplier organization to drive network-level cost savings.
- Partner with Global Technical Operations for strategic partnerships with key suppliers, including contract manufacturers and critical service providers.
- Drive supplier performance management (KPIs, scorecards, governance models).
- Partner with Global Technical Operations to support supply continuity and risk mitigation through robust supplier risk programs and dual/multi-sourcing strategies
Cross-Functional Collaboration
- Partner with Global Technical Operations, Quality, Regulatory, and Supply Chain teams to support product lifecycle, manufacturing scale-up, and commercialization.
- Collaborate with R&D and external innovation teams to enable early supplier engagement and technology scouting.
Risk & Compliance
- Ensure adherence to regulatory requirements (GxP, GMP) and company policies across the supply base.
- Monitor supplier quality and compliance in collaboration with QA/QC teams.
Team Leadership (if Director level)
- Build, lead, and develop a high-performing global sourcing team.
- Foster a culture of accountability, continuous improvement, and stakeholder alignment.
Qualifications
Education
- Bachelor's degree in Supply Chain, Engineering, Business, Life Sciences, or related field required
- MBA or advanced degree preferred
Experience
- Associate Director: 8-10+ years of relevant experience in strategic sourcing/procurement, with exposure to Technical Operations in life sciences
- Director: 12-15+ years of experience, including leadership experience managing global teams and complex supplier networks
- Demonstrated experience sourcing within regulated environments (GMP/GxP)
Industry Expertise
- Strong understanding of pharmaceutical/biotech manufacturing processes and supply chains
- Experience with CMOs/CDMOs, direct materials, and technical services categories
- Knowledge of regulatory and quality requirements in life sciences
Core Competencies
- Strategic thinking and business acumen
- Advanced negotiation and influencing skills
- Supplier relationship and stakeholder management
- Financial acumen (TCO, cost modeling, budgeting)
- Risk management and problem-solving
- Leadership and team development (Director level)
Key Performance Indicators (KPIs)
- Cost savings and value delivery
- Supplier performance (quality, delivery, innovation)
- Stakeholder satisfaction
- Contract compliance and cycle times
Working Environment
- Global role with cross-regional collaboration
- Moderate travel required (10-25%) depending on business needs
About Incyte
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
501 - 1,000 Employees
Headquarters location
Wilmington, DE, US
Year founded
1991