Manufacturing Technician I/II Sunday-Wednesday 6:00am - 4:30pm

PCI TRGR Penn Pharmaceutical Services Ltd; Bedford (NH); On-site; USD 40,000 - 70,000; Full time

Job summary

Ein innovatives Unternehmen sucht einen Manufacturing Technician, der in einem dynamischen Umfeld arbeitet und biopharmazeutische Produkte herstellt. In dieser spannenden Rolle sind Sie verantwortlich für die Durchführung von aseptischen Füllungen, die Bedienung von Produktionsgeräten und die Einhaltung strenger GMP/ISO-Standards. Sie werden Teil eines Teams, das sich für die Entwicklung lebensverändernder Therapien engagiert, und Ihre Arbeit wird einen direkten Einfluss auf die Patientenversorgung haben. Wenn Sie eine Leidenschaft für Qualität und kontinuierliche Verbesserung haben, ist dies die perfekte Gelegenheit für Sie.

Qualifications

• 0-2 Jahre Erfahrung in der pharmazeutischen oder medizinischen Geräteherstellung.
• Fähigkeit, grundlegende Instrumente zu bedienen und Anweisungen zu befolgen.

Responsibilities

• Vorbereitung von Lösungen und aseptisches Füllen von Behältern.
• Betrieb von aseptischen Füll- und Lyophilisierungsausrüstungen.
• Dokumentation der Arbeitsaktivitäten und Einhaltung von SOPs.

Skills

Aseptische Techniken

Dokumentation

GMP/ISO Standards

Kommunikationsfähigkeiten

Mechanische Eignung

Education

High School Diploma oder gleichwertig

Tools

Autoklaven

Zentrifugen

Lyophilisierer

Waagen

Job description

Manufacturing Technician I/II Sunday-Wednesday 6:00am - 4:30pm

Manufacturing Technician I/II Sunday-Wednesday 6:00am - 4:30pm

Apply locations: Bedford, NH, USA | Full time | Posted 2 Days Ago | Job requisition id: JR114031

Life-changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in people who make an impact, drive progress, and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

Summary of Objective:

The Manufacturing Technician I learns and performs a variety of tasks under supervision, following manufacturing instructions compliant with GMP/ISO standards and safety guidelines. Responsibilities include routine and critical manufacturing tasks such as equipment preparation, formulation, aseptic compounding, and filling for biopharma and medical devices, working with Master production records and SOPs, and embodying PCI's Guardian values and behaviors.

Essential Duties and Responsibilities:

1. Maintain safe work habits and adhere to PCI safety procedures.
2. Demonstrate knowledge of aseptic techniques.
3. Prepare solutions, perform aseptic filling, and label vials under sterile and non-sterile conditions.
4. Operate aseptic filling and lyophilizer equipment in controlled environments.
5. Prepare equipment for sterilization and lyophilization.
6. Operate processing equipment such as autoclaves, ovens, vial washers, centrifuges, and mills.
7. Assist in formulation and dispensing of products per SOPs and MBRs.
8. Sanitize production areas and prepare equipment for manufacturing.
9. Complete and maintain documentation of work activities.
10. Follow instructions accurately and document production steps.
11. Identify and escalate deviations, participate in investigations.
12. Maintain cleanliness and order in operational areas.
13. Perform COP, CIP, and SIP to prepare equipment.
14. Review and update SOPs and batch records as needed.
15. Contribute to a positive work environment and participate in media fill/aseptic proficiency testing.

Special Demands:

• Ability to wear PPE such as safety glasses, gloves, and shoes.
• Gowning and entry to controlled areas.
• Lifting up to 25-50 lbs.
• Standing for 6 hours in a production setting.
• Working any shift as required.

Work Environment:

• Interaction with cross-functional teams including QA, QC, Engineering, R&D, and Validation.
• This is an individual contributor role.

Travel: <10%

Note: The role involves adapting to a dynamic environment with complex product mixes, requiring resilience, flexibility, and the ability to handle process variations and client scrutiny.

Qualifications:

• 0-2 years of experience, preferably in pharmaceutical or medical device manufacturing.
• High school diploma or equivalent.
• Ability to weigh, measure, and operate basic instruments.
• Ability to follow instructions and seek help for complex tasks.
• Good communication skills and mechanical aptitude.
• Commitment to ethical standards and continuous improvement.
• Honesty, integrity, and respect.
• Resilience and ability to work in a fast-paced environment.

Join us and be part of building the bridge between life-changing therapies and patients. Let’s talk about the future.

EEO Statement:

PCI Pharma Services is an Equal Opportunity Employer. We do not discriminate based on race, color, religion, age, sex, or other protected statuses. We are committed to an inclusive workplace and continuous assessment of our practices to foster belonging and growth for everyone.

About Us

Why work for PCI Pharma Services?

We focus on quality, operational excellence, and delivering an outstanding customer experience. Our people are our strength, and we strive to create a culture of purposeful work, learning, and growth, supported by a fair rewards program. We believe in our purpose and our people, fueling our business.