Pharma Production Operator - Day Shift & Benefits

Kindeva; Loughborough; On-site; GBP 26,000 - 32,000; Full time

Benefits offered by this job

Shift premium 8%

Company pension (up to 10% employer)

Private medical insurance

Life assurance 4x salary

Free on-site parking

Cycle to work

Job summary

Kindeva Drug Delivery in Loughborough is expanding its pharmaceutical manufacturing team and seeks motivated individuals to join the inhalation production line. You will operate in a highly controlled environment, follow cGMP, and participate in achieving production targets through precise documentation and process discipline.

Full training will be provided, with emphasis on safety, ALCOA records, and continuous improvement.

Qualifications

• GCSE Maths & English Grade C/Level 4 or above (preferred).
• Experience of working in a production environment, on a shift basis.
• Good understanding of GMP is preferable.
• Computer literate, familiar with Microsoft Word and Excel.

Responsibilities

• Working in a collaborative environment to ensure that production and changeover targets are met.
• Following all procedures and processes within the department to maintain a high standard of cGMP and that everything is completed correctly first time.
• Health and safety is the responsibility of everyone and is vital across the whole site, not just within the production areas.
• Accurate records and paperwork are needed within a timely manner, following the principles of ALCOA.
• We are frequently looking at continuous improvement ideas, and suggestions are proactively welcomed and discussed.
• Flexibility will be required dependant on the department’s needs.

Skills

Teamwork

Communication

Time management

Interpersonal skills

Flexibility

Education

GCSE Maths & English (Grade C/4 or above)

Tools

Word

Excel

Job description

Kindeva Drug Delivery in Loughborough is expanding its pharmaceutical manufacturing team and seeks motivated individuals to join the inhalation production line. You will operate in a highly controlled environment, follow cGMP, and participate in achieving production targets through precise documentation and process discipline.

Full training will be provided, with emphasis on safety, ALCOA records, and continuous improvement.