Biotechnologist I - GMP Manufacturing (Day Shift)

Lonza

Slough

On-site

Confidential

Full time

3 days ago
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Benefits offered by this job

Agile culture
Inclusive workplace
Compensation programs
Benefits by role

Job summary

Lonza in Slough is seeking a Biotechnologist for day shift on a 12-month FTC to join our GMP manufacturing team. This entry-level role provides hands-on experience in a controlled cleanroom environment, focusing on producing life-changing medicines with high quality and safety standards.

You will learn production systems, complete required training, and work closely with colleagues to ensure on-schedule manufacturing while adhering to cGMP procedures.

Qualifications

  • Manufacturing or Production experience is desirable.
  • Good command of both written and oral English, essential for effective collaboration and documentation.
  • Outstanding organizational skills to manage tasks efficiently and meet deadlines.
  • Strong problem-solving abilities to address and resolve challenges promptly.
  • Established track record of strong interpersonal abilities, providing guidance and mentorship to promote teamwork and facilitate team growth.
  • Maintain meticulous attention to detail to ensure the highest standards of work quality.
  • Cultivate a collaborative and inclusive environment, displaying respect and support for your colleagues.
  • Be flexible and open to change, demonstrating a proactive approach to evolving situations.

Responsibilities

  • Successfully implement various tasks to ensure products are manufactured according to schedule, safety requirements, and Good Manufacturing Practices (GMP).
  • Acquire a detailed understanding of production systems and relevant Lonza systems to enable efficient production. Ensure completion of all necessary training to perform production activities with precision.
  • Adhere strictly to high standards of cGMP for both yourself and your colleagues. Gain familiarity with Lonza's quality procedures, including change control, the deviation system, and validation procedures.
  • Assist in correction and data management activities, ensuring that documentation standards are met impeccably.
  • Engage directly in the manufacturing process, identify continuous improvements, and contribute to the completion of various projects.
  • Uphold high standards of housekeeping, team values, and safety policies. Highlight safety issues and foster a safety-first attitude within the team. Ensure objectives are met within the designated timeframe.

Skills

Manufacturing experience
Written English
Oral English
Organizational skills
Problem solving
Interpersonal skills
Attention to detail
Collaborative environment
Adaptability

Job description

Lonza in Slough is seeking a Biotechnologist for day shift on a 12-month FTC to join our GMP manufacturing team. This entry-level role provides hands-on experience in a controlled cleanroom environment, focusing on producing life-changing medicines with high quality and safety standards.

You will learn production systems, complete required training, and work closely with colleagues to ensure on-schedule manufacturing while adhering to cGMP procedures.

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