Bioprocess Hardware Specialist

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

This Bioprocess Hardware Specialis is focused on the reliability, operation, and optimization of manufacturing skids within a clinical production environment. The successful candidate will be responsible for ensuring that upstream, downstream, and fill-finish systems remain fully operational, serving as the primary technical expert for hardware and software performance, chemical safety, and equipment integrity.

How You’ll Spend Your Day

⦁ Provide technical oversight and maintenance support for upstream (bioreactors), downstream (chromatography, filtration), and fill-finish clinical production skids.

⦁ Perform advanced troubleshooting of hardware and software issues to maximize uptime and ensure the stability of clinical manufacturing runs.

⦁ Monitor and optimize equipment performance and engineering process flows to meet clinical production timelines.

⦁ Oversee the cleaning and maintenance of process skids (CIP/SIP), ensuring all protocols align with validated clinical standards and safety requirements.

⦁ Apply a deep understanding of chemical reactions and safety protocols to manage hazardous materials and ensure a safe, compliant operating environment.

⦁ Collaborate with cross-functional teams to implement equipment upgrades and process optimizations specific to clinical scale-up.

⦁ Lead the documentation of technical equipment issues, root cause analysis, and corrective actions (CAPA) within the clinical quality system.

⦁ Provide technical guidance and training to operators on equipment handling, control interfaces, and safety procedures.

⦁ Support validation and commissioning activities for new skids or modified manufacturing hardware.

Your Skills and Experience

⦁ Bachelor’s degree in Chemical Engineering, Bioengineering, Biotechnology, or a related scientific field.

⦁ A minimum of 5 years of professional experience in the biologics pharmaceutical industry, with a focus on clinical manufacturing environments.

⦁ Demonstrated expertise in troubleshooting and optimizing automated manufacturing systems (both hardware and software/control logic).

⦁ Thorough understanding of cGMP regulations, chemical safety standards, and specialized cleaning protocols for pharmaceutical skids.

⦁ Proven ability to manage the technical and operational complexities of manufacturing equipment.

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 holiday.

• 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.

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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 [email protected] 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.

Important notice to Employment Agencies - Please Read Carefully

Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities.  All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.