QC Sample Management Associate

Teva; West Chester (Chester County); Sur place; USD 52 000 - 76 000; Plein temps

Résumé du poste

Teva in West Chester, PA is seeking a Sample Management Associate to support QC operations in a GxP environment. You will handle receipt, inventory, distribution, shipping, and disposal of analytical samples, and coordinate testing with external labs.

The role requires a BS in a scientific discipline or 2–4 years of pharma QC lab experience, hands-on bench chemistry, meticulous attention to detail, and strong written and verbal communication.

Qualifications

• BS in a scientific discipline with 0–2 years in pharma QC laboratory.
• Willing to learn and take ownership of the position.
• Effective written and oral communication skills are essential.

Responsabilités

• Support sample management activities, including receipt, inventory, distribution, shipping, and disposal of analytical samples.
• Prepare analytical and stability samples and coordinate testing with external laboratories.
• Assist in sterile aliquoting of samples in a biosafety cabinet.
• Maintain and track laboratory inventory using the LIMS Inventory Manager.
• Enter and maintain sample and testing data in LIMS.
• Support environmental chamber monitoring, alarm response, maintenance, and compliance activities.
• Assist with the development, review, and revision of SOPs, work instructions, and forms.
• Maintain compliance with ICH, GxP, and safety requirements, escalating deviations, unexpected results, and equipment issues as needed.
• Document and communicate results clearly in written and verbal formats.
• Maintain collaboration with external testing partners and cross-functional teams.
• Contribute to a clean, safe, and compliant laboratory environment.
• Provide feedback on systems and processes to promote continuous improvement.

Connaissances

Oral communication

Written communication

Attention to detail

Lab experience

Formation

BS degree in science

Outils

LIMS Inventory Manager

Description du poste

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

The Sample Management Associate position is ideal for entry level candidates seeking to gain experience in the pharmaceutical industry. This position supports Quality Control operations in a GxP-compliant environment through QC sample management, laboratory sample administration, and GMP stability program activities. The role requires hands-on bench chemistry experience, a basic understanding of biopharmaceutical development and GxP regulations, and strong attention to detail. Candidates must be capable of working independently, managing multiple priorities simultaneously, and performing tasks in accordance with written procedures. Additional responsibilities include supporting stability studies and monitoring environmental chambers. This position will include both lab-based and desk-based work. New graduates are encouraged to apply.

How You’ll Spend Your Day

• Support sample management activities, including receipt, inventory, distribution, shipping, and disposal of analytical samples
• Prepare analytical and stability samples and coordinate testing with external laboratories
• Assist in sterile aliquoting of samples in a biosafety cabinet
• Maintain and track laboratory inventory using the LIMS Inventory Manager, ensuring accurate recordkeeping and material availability
• Enter and maintain sample and testing data in LIMS
• Support environmental chamber monitoring, alarm response, maintenance, and compliance activities.
• Assist with the development, review, and revision of SOPs, work instructions, and forms.
• Maintain compliance with ICH, GxP, and safety requirements, escalating deviations, unexpected results, and equipment issues as needed.
• Document and communicate results clearly in written and verbal formats.
• Maintain collaboration with external testing partners and cross-functional teams.
• Contribute to a clean, safe, and compliant laboratory environment.
• Provide feedback on systems and processes to promote continuous improvement and champion selected change
• This role will be exposed to various groups in the Quality Control department including stability, chemistry, raw materials, and potency.

Your Skills and Experience

• BS degree in a scientific discipline with 0-2 years of experience in a pharmaceutical QC laboratory, or in lieu of a degree, 2-4 years of experience in a pharmaceutical QC laboratory. Any equivalent combination of education, training, and/or experience that fulfills the requirements of the position will be considered.
• A successful candidate will be eager to learn and will take ownership of the position, looking for ways to improve the process.
• Effective written and oral communication skills are essential.

How We’ll Take Care of You

We offer a competitive benefits package, including:

• Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
• Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
• Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.
• Life and Disability Protection: Company paid Life and Disability insurance.
• Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.

The total compensation may also include restricted stock units and discretionary awards, depending on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Request a reasonable accommodation by sending an email to [e-mail] with the nature of your request and your contact information. Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address.