ZipRecruiter

Log In

1

Assistant Biotech Quality Control Jobs in Delaware

WuXi AppTec

Production Operator I

Middletown, DE · On-site

$15.75 - $19/hr

... * Assist with basic troubleshooting; partner with Maintenance/Engineering for repairs and PMs ... Collaborate with QA, QC, MSAT/Process Engineering, Supply Chain, Facilities, and EHS.

WuXi AppTec

Production Operator I

Middletown, DE

$15.75 - $19/hr

... * Assist with basic troubleshooting; partner with Maintenance/Engineering for repairs and PMs ... Collaborate with QA, QC, MSAT/Process Engineering, Supply Chain, Facilities, and EHS. * Bachelor ...

Merck & Co.

... Quality Control/Assurance, Supply Chain or Planning, Regulatory Affairs, Safety, and R&D to provide ... Bachelor of Science in Chemical Engineering, Biotechnology, Mechanical Engineering, Biochemistry ...

MSD

Sr. Specialist, Engineering

Millsboro, DE

... Quality Control/Assurance, Supply Chain or Planning, Regulatory Affairs, Safety, and R&D to provide ... Bachelor of Science in Chemical Engineering, Biotechnology, Mechanical Engineering, Biochemistry ...

Datwyler

Laboratory Technician 3rd Shift

Middletown, DE · On-site

$18 - $23.75/hr

Summary The Laboratory Technician is a critical member of the Quality Control team, ensuring the ... Biotech, or Medical Device). • Technical Skills: o Proficiency in MS Office and SAP. o ...

previous page

Showing results 41-60

All JobsBiotech Quality Control JobsAssistant Biotech Quality Control JobsAssistant Biotech Quality Control Jobs in Delaware

Assistant Biotech Quality Control information

What is the difference between Assistant Biotech Quality Control vs Laboratory Technician?

AspectAssistant Biotech Quality ControlLaboratory Technician
CredentialsAssociate degree or equivalent, relevant certificationsAssociate degree or diploma, technical training
Work EnvironmentBiotech labs, quality assurance settingsResearch labs, clinical or industrial labs
Employer & IndustryBiotech companies, pharmaceutical firmsResearch institutions, healthcare, manufacturing
Common TasksSample testing, data recording, quality checksSample preparation, equipment operation, data collection

Assistant Biotech Quality Control and Laboratory Technicians both work in laboratory settings, often with overlapping skills. However, quality control roles focus more on ensuring product standards and compliance, while laboratory technicians may be involved in broader research or testing tasks. Understanding these differences helps job seekers target the right roles in the biotech industry.

What are popular job titles related to Assistant Biotech Quality Control jobs in Delaware? For Assistant Biotech Quality Control jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Assistant Biotech Quality Control jobs in Delaware look for? The top searched job categories for Assistant Biotech Quality Control jobs in Delaware are:
What cities in Delaware are hiring for Assistant Biotech Quality Control jobs? Cities in Delaware with the most Assistant Biotech Quality Control job openings:
Assistant Biotech Quality Control jobs near you
Infographic showing various Assistant Biotech Quality Control job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.

Production Operator I

WuXi AppTec

Middletown, DE • On-site

$15.75 - $19/hr

Other

Re-posted yesterday

Job description

Overview
Operator I supports cGMP pharmaceutical manufacturing activities by executing batch operations, cleaning and setup, in-process checks, and documentation with a strong focus on safety, quality, and right-first-time performance. This role is fully trained to operate designated equipment and to work effectively within a cross-functional team in a regulated environment.
Responsibilities
Production Operations
  • Perform manufacturing steps per approved batch records (e.g., dispensing, measuring, charging, mixing, filtration, filling, capping, packaging etc.) and record results contemporaneously.
  • Set up, operate, and monitor assigned equipment (e.g., blenders, tablet presses, coaters, encapsulators, roller compactors, fluid bed dryer, mills etc.) within validated parameters.
  • Conduct and document in-process checks (pH, weight/volume, torque, visual inspection etc.) and make routine adjustments under supervision.
  • Execute line clearances and support changeovers, including equipment assembly and disassembly between production batch runs to minimize downtime.
  • Work in classified areas (ISO 8-7) following aseptic techniques and environmental monitoring practices.
  • Complete initial and periodic gowning qualifications; perform routine interventions per procedure.
  • Perform equipment and area cleaning (CIP/SIP/manual) and document to meet cleanliness status/line clearance.
  • Assist with basic troubleshooting; partner with Maintenance/Engineering for repairs and PMs.

Documentation & Quality
  • Complete batch records, logbooks, and forms accurately and legibly; reconcile materials and yields.
  • Initiate notifications for deviations, OOS/OOT, or atypical events; support investigations and CAPAs as needed.
  • Participate in audits, room/equipment release, and lot sampling activities.
  • Meet or exceed KPIs (Right-First-Time, schedule adherence, yield, 5S audit scores etc.).
  • Suggest and help implement process and documentation improvements (lean, 5S, SMED).
  • Collaborate with QA, QC, MSAT/Process Engineering, Supply Chain, Facilities, and EHS.

Qualifications
  • Bachelor's or technical certificate in a science/technical field preferred.
  • Experience working with tablet presses, encapsulators, fluid bed dryers, roller compactors, blenders, coaters and/or other pharmaceutical manufacturing equipment is required.
  • Minimum of 3 years in GMP manufacturing, food/beverage, biotech, medical device, or similar regulated/industrial setting preferred (new-grad friendly).
  • Experience assisting in regulatory inspections and audits.
  • Ability to work in a fast-paced, highly regulated environment.

Knowledge / Skills / Abilities:
  • Fundamental understanding of cGMPs, cleanroom behaviors, and data-integrity expectations.
  • Ability to learn and operate production equipment and read P&IDs, batch records, and SOPs.
  • Basic math and measurement skills; able to use scales, pH meters, and hand tools.
  • Computer literacy; experience with MES/LIMS/ERP and electronic logbooks a plus.

Physical & Work Environment Requirements:
• Stand/walk for extended periods (8-12 hour shifts); lift/push/pull up to 50 lbs.
• Work in controlled environments; wear PPE (gowning, gloves, safety glasses, face coverings, hearing protection as applicable).
• Exposure to chemicals, sanitizers/disinfectants, and routine noise levels within regulated limits
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

Apply