Job Details

ID #51635525
Estado New York
Ciudad Norwich
Full-time
Salario USD TBD TBD
Fuente Actalent
Showed 2024-05-06
Fecha 2024-05-07
Fecha tope 2024-07-06
Categoría Etcétera
Crear un currículum vítae
Aplica ya

QC Team Leader

New York, Norwich, 13815 Norwich USA
Aplica ya

Actalent Scientific is HiringDescription:The Team Leader Quality Control: Leads and manages activities supporting the laboratory function in executing daily operations and testing necessary to support commercial products. Anticipates and resolves problems independently while conforming to SOPs and GMP regulations Monitors the scientific and financial progress of projects that they are assigned May have responsibility for a laboratory group or function and may have direct reportsOrganization Structure:The Team Leader Quality Control reports to the Manager Quality Control or Director QC. Any of the following Quality Control staff may report to the Team Leader Quality Control: Chemist-analyst 1, 2, and 3 Microbiologist 1, 2, and 3 MetrologistsResponsibilities:Primary responsibilities of this role include the following:

Safety

o Participate in weekly/monthly safety training, identify potential safety hazards, implement appropriate safety improvements and take part with investigations of safety related incidents o Perform job functions in a safe manner consistent with site safe practices and regulatory (e.g. -OSHA) requirements

Compliance

o Conduct assigned tasks in compliance with cGXP requirements, current industry standards, compendial standards, FDA expectations and internal procedureso Ensure investigations are conducted in a timely manner and are completed within established target completion dates o Ensure that the Quality Control staff have been appropriately trained before performing a GMP task

Productivity

o Serve as primary resource for planning and scheduling of tests o Assist analysts as needed and troubleshoot if required o Witness analytical notebooks of peerso Conduct testing consistent with established methods/procedureso Schedule and/or perform necessary validation, qualification and calibration of laboratory equipment/instrumentso Schedule method development, qualification, verification or validation according to established SOPs as well as FDA/USP/ICH guidelineso Custodian of laboratory systems and is proactive in implementing significant system improvements and / or laboratory procedureso Communicate with clients, contractors, and regulatory agents as requiredo Provide leadership and guidance to laboratory system owners and removes barriers to enable positive changeo Function as the laboratory representative on multi-department project teams o Familiar with department and plant systems and effectively operates within systems to achieve desired resultso Serve as backup to the Manager, Quality Control

Staff Development / Training

o Identify areas of improvement in laboratory testingo Provide technical training to analysts

Leadership

o Lead by example, demonstrate through example the expected professional conduct, display integrity and honesty, inspire staff to excel and foster an environment of continuous improvemento Assist management with supervising project task as neededSkills:quality control, laboratory, chemistry, biology, microbiology, gmp, quality assuranceAdditional Skills & Qualifications:o BS in Chemistry, Biochemistry, Biology or Microbiology or related disciplineo 5+ years experience in a laboratory environment (quality control or similar pharmaceutical industry experience preferred), or MS in Chemistry, Biochemistry, Biology or Microbiology or related discipline and 3+ years experience o Thorough understanding of cGMP requirements o Strong communication, interpersonal, and organizational skillso Ability to work with a sense of urgency in a fast-paced environment o Strong technical writing and investigational skillsGMP DECISION-MAKING AUTHORITYThe Team Leader Quality Control is responsible for decisions related to: o When an investigation is warrantedo When analyst training is warrantedo Disposition of laboratory test results and samples/batcheso Prioritization of staff work assignments and testing scheduleso Suitability of analytical equipment/instruments for useo When a Change Control is warrantedo When an analyst is qualified to perform testingo Applies advanced theoretical knowledge, education, experience, and training in conjunction with technical resources to troubleshoot and resolve problemsAbout Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.

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