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Associate Director Quality Control Jobs

Director Of Quality Control
By Rx Group At Florida, United States
5+ years of people management experience with proficiency in establishing objectives, monitoring performance, providing feedback, and developing staff.
Excellent verbal and written communication skills and ability to communicate effectively with site personnel, peers and management.
Solid time management skills and ability to handle multiple tasks and deliver high quality results within set timelines.
Manage Quality Control Microbiology staff including recruiting, onboarding, and performance management.
Escalate challenges to management; develop constructive proposals and implement solutions for resolution of challenges.
Ensure compliance within QC by monitoring test methods, SOPs, and QC analytical data to cGMPs, pharmacopeial and regulatory requirements.
Payment Processing - Quality Control Associate
By Alleviate Financial Solutions At California, United States
Energetic working environment, both in-person and remote
Minimum of 2 years of customer service experience preferred
Customer service phone experience preferred
Excellent customer services and clear verbal communication skills
Knowledgeable of MS Office: word, excel, outlook
This position must pass a post-offer pre-employment criminal background check.
Director Of Quality Control
By Blue Nile At Greater Syracuse-Auburn Area, United States
Excellent leadership and management skills, with the ability to motivate and guide teams to achieve high levels of performance.
Strong project management skills, with the ability to manage multiple projects and initiatives simultaneously.
Create and drive KPI’s for QC department to ensure time management, quality, and customer satisfaction are met.
Collaborate with internal team members in Supply Chain Management, Production, and Merchandising.
Manage the quality control teams and implement and propose new corrective actions to improve the quality of product.
Strong analytical and problem-solving skills, with the ability to identify and resolve complex quality issues.
Associate Director, Quality Control
By BioSpace At Concord, NC, United States
Supervise, coach, and aid in employee development and performance management; ensure a fair and equitable work environment
Establish a lab operation compliant with Lilly Global Quality Standards and regulatory requirements, including establishing lab practices, procedures, test methods, etc.
Bachelor of Science in Biology/Microbiology or related work experience
Minimum 5 years of pharmaceutical leadership experience including leading or working effectively with a cross functional groups
Minimum 5 years GMP lab experience including microbiological testing, environmental monitoring, and method transfer
Deep understanding of compliance requirements and regulatory expectations
Quality Control Associate Jobs
By ImmPACT Bio At Los Angeles, CA, United States
Previous working experience in the lab, sample management, aseptic techniques, and cell culture activities are highly recommended.
Executes QC sample management activities, which include receipt, inventory sample entry, sample distribution, sample label creation, sample coordination/shipment preparation, and disposal.
Performs routine maintenance of laboratory reagents/materials orders and inventory management.
Should be able to manage the workload, meet deadlines, be eager to learn new techniques, and demonstrate good organizational skills.
Basic understanding of Good Laboratory Practices (GLP) with strict adherence to cGMP requirements is essential.
Dependable, able to learn new skills rapidly, and able to work well within the team.
Quality Control Associate Ii
By BioLegend At San Diego, CA, United States
Minimum Qualifications – Education And Experience
Preferred Qualifications – Education And Experience
Other projects or responsibilities as may be required.
1-3 years of previous experience in a laboratory setting
Familiarity with basic lab equipment and knowledge of lab safety protocols
Excellent organization, communication, and problem solving skills
Senior Associate Director, Quality Control
By Boehringer Ingelheim At , Athens, 30601, Ga
Excellent reading / writing and communication skills.
Must be willing to take a drug test and post-offer physical (if required)
Responsible for compliance with industry guidelines and governmental regulations, preparing, auditing, and reviewing test methods, test records and other GMP
Documentation, hosting inspections and audits of the QC areas. Establishes and maintains quality agreements with vendors, third-party manufacturers, and contractors.
Directs the oversight of data integrity with instrumentation and manual processes used throughout the Quality Control laboratories.
Responsible for compliance with industry guidelines and governmental regulations, preparing, auditing, and reviewing method test records and other GMP
Quality Control Associate Ii
By Revvity At , San Diego, Ca $28 - $35 an hour
Preferred Qualifications – Education and Experience
Other projects or responsibilities as may be required.
1-3 years of previous experience in a laboratory setting
Familiarity with basic lab equipment and knowledge of lab safety protocols
Excellent organization, communication, and problem solving skills
Experience with some of the following applications: flow cytometry, western blotting, Immunoprecipitation, bioassays, ELISA and IHC/ICC
Quality Control Associate Ii (Chemistry) (Archived)
By GXPeople At , , Ma
At least 2 years’ experience working in a laboratory.
A great compensation and benefits and a full relocation package is available for you and your family.
A Bachelor’s or Master’s Degree in a Scientific field.
Please apply if you have:
For more information, please contact Mags Wosik at [email protected] or submit the form below.
N.B. This role is currently open to US residents and Green Card holders.
Quality Control Associate Ii
By Corning At , Glendale, 85301, Az
High School or General Education Diploma
Read and interpret production travelers and engineering specifications to ensure product conformance at each manufacturing product sequence.
Document part characteristics and measurements on inspection history cards during first article inspections and other inspection sequences.
Record data from inspection history cards on inspection files and maintain accurate and legible inspection records.
Load and/or transport part containers utilizing a forklift, hand truck or manual/motorized pallet jack to assigned locations.
Determine quality (Pass/Fail) of manufactured parts based on dimensional and visual inspection.
Quality Control Associate Jobs
By Glanbia Foods At , Salt Lake City, 84104, Ut

Reporting to the Corporate Director, Quality and Regulatory Affairs JOB SUMMARY Responsible for streamlining the operations in the tower and ensuring the area is appropriately sanitized. ESSENTIAL ...

Clinical Research Quality Control Associate
By Clinilabs inc At , New York, 10019, Ny $22 an hour
Provide support (e.g. data entry, filing, QC, etc…) to CRU personnel and other Clinilabs personnel ad requested and needed.
Manage and track project timelines and quality issues.
Must have related experience for at least two years.
Must possess excellent clerical, strong computer and good interpersonal skills.
Reading and understanding study protocols.
Communicate with all operational departments regarding project status/issues.
Associate Ii, Quality Control
By Biogen At , Research Triangle Park, 27560, Nc
Understanding of scientific principles, ability to communicate with peers and management
Participates in the execution of method/material qualification and analytical improvement projects.
3+ years of relevant experience (B.S. Degree), 6+ years of relevant experience (A.S. degree)
Solid working knowledge of operations/quality systems utilized in QC operations/support teams (e.g. strong test method/scientific base)
Provides timely review of data and documentation generated for or by QC.
Ability to perform color differentiation testing
Quality Control Associate I
By Exact Sciences Corporation At , Madison, 53719, Wi $41,000 - $66,000 a year
Support the Operations department in other non-laboratory functions, as determined by Operations management.
Perform other related duties as assigned by management.
Support and comply with the company’s Quality Management System policies and procedures.
Strong documentation skills in accordance with GMP requirements.
Evidence of strong analytical and problem-solving skills, and ability to make decisions with limited information and operate with autonomy.
Excellent oral and written communication and interpersonal skills.
Associate Director, Quality Systems
By Gilead Sciences At , Foster City, 94404, Ca $172,890 - $223,740 a year
Responsible for investigation management of critical, major, and minor investigations related to GxP operations.
Supports management review process through development, generation, and review of quality system metrics and trending, and escalate issues as required.
Manages QA personnel, including organizing and prioritizing daily tasks, performing training, and writing performance reviews.
Performs a wide variety of activities to ensure compliance with applicable quality objectives and regulatory requirements.
Bachelors Degree and 10+ years of experience required OR
Masters Degree and 8+ years of experience required OR
Quality Control Associate Jobs
By Printful At , Charlotte, Nc
Communicating policies, procedures, requirements, and safety information to teammates as needed
Have strong communication and interpersonal skills
Multi-task and manage your time efficiently
Competitive pay and benefits: health, dental, vision, and life insurance
Examining items and detecting errors to ensure we’re producing top-quality products for our customers
Detecting inconsistencies in printer machine settings to spot recurring issues and keep production running smoothly
Director, Quality Control Jobs
By Bachem At , Vista, 92081, Ca $141,892 - $195,102 a year
At least 3 years management experience required
Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues
Oversee and conduct cGMP, ICH and ISO stability programs to comply with regulatory requirements
Oversee work of direct reports; distribute workload, and cross-train staff on different quality areas. Interview, hire, train, develop and manage employees
Master's Degree in Chemistry or Chemical Engineering with a minimum of 5 years’ work experience in GMP manufacturing required or
Bachelor's Degree in Chemistry or Chemical Engineering with a minimum of 8 years’ work experience in GMP manufacturing required
Director, Quality Control Jobs
By Alexza Pharmaceuticals At , Fremont, 94555, Ca From $199,000 a year
Excellent written, oral communication skills, and experience with computer software such as WORD, EXCEL, etc.
Highly organized, detail-oriented, capable of multi-tasking, strong interpersonal skills in order to collaborate with individuals in a matrix environment.
Strong knowledge of QC testing of small molecule drugs in a compliant cGMP setting.
10+ years of relevant experience in a cGMP pharmaceutical QC environment, or 8+ years with a Master’s degree.
Experience in a commercial environment highly desirable.
Starts at $199,000 and is commensurate with experience
Quality Control Associate Jobs
By UC San Diego Health At , San Diego, 92093, Ca $59,000 - $85,000 a year
Experience using basic laboratory equipment; knowledge of safe laboratory procedures.
Hands-on experience in a pharmaceutical, biotech, drug manufacturing, or academic environment is required, with knowledge of clean room practices being essential.
Six (6) years of relevant experience or a Bachelor's degree in a related field plus two (2) years of related/relevant experience.
Working knowledge of research function. Knowledge of test methods used to test cell therapy products or similar characterization assays.
Skills to communicate complex information in a clear and concise manner both verbally and in writing.
Working skills in analysis and consultation. Strong analytical and critical thinking skills, with the ability to quickly analyze problems.
Microbiology Quality Control Associate (Biologics Cmc)
By Teva Pharmaceuticals At , West Chester, 19380, Pa
Maintain compliance with applicable ICH, GMP and safety regulations. Notify management of unexpected results, procedural deviations and equipment problems.
Process environmental monitoring samples including plate enumeration and data entry.
Perform release and stability testing and record data per GxP requirements.
Participate in and may assist in writing laboratory investigations.
Participate in aseptic processing in a clean room environment.
Actively contribute to the maintenance of a clean, safe working environment in the laboratories.