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Pharmaceutical Technician II- Day Shift

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Catalent

2021-12-03 11:30:03

Job location Winchester, Kentucky, United States

Job type: fulltime

Job industry: Science & Technology

Job Contact: Click apply

Job description

Military Veterans are Encouraged to Apply.

Job Description

Position Overview:

Catalent hires people with a passion to make a difference to the health of millions of people globally. Your expertise, coupled with Catalent's advanced technologies and collaboration with thousands of innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents, ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. Interested in learning more about life at Catalent? Start here

Pharmaceutical Technician II- Day Shift

The Pharmaceutical Technician II reports to the Manufacturing Supervisor.

Pharmaceutical Technicians II are primarily responsible for the manufacturing of pharmaceutical product per established specifications. These responsibilities include weighing, transferring, mixing, and processing of raw material to create a finished good, as well as a variety of support activities, such as cleaning of production rooms, corridors, and equipment. Pharmaceutical Technicians II operate with a high level of independence and can perform all the activities pertaining to the manufacturing of product, such as setups, machine processing, troubleshooting, and reacting to issues, in at least one production room. All responsibilities are dictated by strict regulations (eg, cGMP, SOP, batch records).

Catalent's Winchester location is the flagship US manufacturing location for large scale complex controlled release (CR) oral dose forms, with integrated analytical and development services. With 20 years of expertise in product development, technology transfers and commercial manufacturing, and roots in industry leading Glatt technology. This site offers newly installed Fluid Beds, expanded analytical labs, and an advanced open facility design that provides flexibility in supporting the requirements of any new customer program.

If you share a passion for patient care in the growing world of pharmaceutical manufacturing and would like to be part of a global drug development and delivery leader, then this might be for you!

This is a 12- Hour Day Shift Position, working hours: 6:00 AM- 6:00 PM. (rotating between working 36 hours in one week and 48 hours in the following week).

The Role

  • Safety & Compliance
    • Understand and follow all environment, health, and safety requirements; in particular, personal protective equipment (PPE) requirements.
    • Always work in a safe manner.
    • Understand and follow all current Good Manufacturing Practices regulations (cGMP), applicable standard operating procedures (SOP), and executed batch records.
    • Complete all required training and qualifications regarding the role in a timely manner; in particular, ComplianceWire assignments.
  • Primary Manufacturing Activities
    • Weigh and transfer materials using calibrated scales and balances.
    • Utilize hand tools to assemble and disassemble various types of machinery.
    • Perform basic calculations with aid of a calculator.
    • Accurately complete all applicable documentation pertaining to completed tasks; in particular, batch records, forms, and cleaning records.
  • Ensure accurate and adequate documentation in production room through label verifications, batch record reviews, etc.
    • Perform detailed cleaning of manufacturing suites and equipment using various cleaning solutions and in accordance with cleaning records.
    • Maintain a work environment that is clean, organized, and audit-ready.
  • Problem Solving, Decision Making, & Independence
  • Independently process any batch from start to finish in at least one processing room/suite.
  • Complete all setup activities without guidance on a large number of processes.
  • React to process issues appropriately and take proper measures to maintain product quality.

The Candidate
  • Minimum of a High School Diploma.
  • Two-year technical or Associate's Degree preferred, or equivalent experience.
  • Prior experience working in a pharmaceutical, biotech or food manufacturing environment (regulated by GMP standards and requirements) is preferred; with specific experience in oral solid dosage manufacturing (fluid bed, granulation, blending, compression, pan coating, or encapsulation manufacturing processes).

Position Benefits
  • Potential for career growth within an expanding Winchester Site
  • Medical, Dental, Vision and 401K are all offered from day one of employment
  • 19 days of paid time off annually + 8 paid holidays

Leadership Competencies for Performance and Development
  • Leads with Integrity and Respect
  • Delivers Results
  • Demonstrates Business Acumen
  • Fosters Collaboration and Teamwork
  • Champions Change
  • Engages and Inspires
  • Coaches and Develops

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

Catalent is committed to the health and safety of its employees, visitors and the customersand patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone's safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.

personal initiative. dynamic pace. meaningful work.
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C atalent is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation or gender identity. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to (see below) . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives:Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to (see below) for us to investigate with local authorities.

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