We are a global contract manufacturing and development organisation. We are recognised experts in liquid and semi-solid capsule products offering expertise in all aspects of the development and manufacture of pharmaceuticals for oral drug delivery.
Our Vision:
Our vision is to be the leading and most trusted, reliable and innovative Europe-based CDMO by upholding the highest industry standards and exceeding customer expectations, while driving strong, sustainable growth for the company.
We are offering new and exciting roles to support the continued expansion of our manufacturing facilities which are required to meet growing market demand.
We are looking for enthusiastic, hard-working people who are willing to learn new skills and have a positive, pro-active approach. Previous experience of pharmaceutical manufacture is not essential, but you must be prepared to work in a cleanroom environment and ensure compliance with GMP regulations at all times.
Key Responsibilities:
· Manufacture of pharmaceuticals products for commercial and clinical trial applications· Ensuring all activities are undertaken in accordance with cGMP, Health and Safety standards, and current SOPs
· Recording data appropriately in batch records and supporting documentation
· Maintaining hygiene standards in all production areas
· Supporting production activities through each stage of the manufacturing process (cleaning, mix preparation, capsule filling and sorting, blister and bottle packing)
· Set-up, operation and strip down of modern high speed production equipment
· Working flexibly within a team to ensure adherence to the production schedule
· Maintaining personal training records
Person Specification:
- Previous experience of pharmaceutical manufacture or working in a cleanroom environment would be an advantage (but not essential)
- Be conscientious and have a good eye for detail - to conduct quality checks and ensure data is accurately recorded
- Be flexibile - to ensure production output and client demands
- Have a high degree of integrity - to maintain compliance with GMP regulations
- Be reliable, and able to make a positive contribution to the production team
- Previous GMP (Good Manufacturing Practice) experience
- Good practical skills
- Demonstrates good literacy and numeracy skills
Please note: Only candidates with permanent Right to Work in the UK will be considered.
NextPharma is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.
Job Type:
· Full Time, Shift Work (Day/Back)
In return we offer:
Competitive salary with attractive benefits package
Private Medical Insurance and Health Cash Plan
Group Personal Pension Plan
Life Assurance
Generous leave entitlement
A friendly and focused working environment
Career development opportunities
Job Type: Temporary
Contract length: 6-12 months
Expected hours: 37.5 per week
Benefits:
- Company pension
- Cycle to work scheme
- Free parking
- Health & wellbeing programme
- Life insurance
- On-site parking
- Private medical insurance
- Referral programme
Schedule:
- 8 hour shift
- Monday to Friday
Ability to commute/relocate:
- Livingston EH53 0TH: reliably commute or plan to relocate before starting work (required)
Work authorisation:
- United Kingdom (required)
Work Location: In person
