Effectively generate new business leads and opportunities from various sources and engage through proper prospecting, email campaigns, cold-calling and regular follow-ups
Knowledge of microbial testing for injectable products and environmental monitoring for sterile manufacturing area. Knowledge of instruments & equipment, method validations, finished dosage and RM testing
M.Pharm, B.Pharm, M.Sc, B.Sc; Responsible for accurate production and packaging changeovers as per packaging schedule. Maintain a clean work area and clean equipment before and after shift.
Unique Pharmaceuticals Limited is a pioneer in the pharmaceutical industry in Nigeria. We have been serving the healthcare sector since 1988 through the production & distribution of quality pharmaceutical products, notably I.V. Fluids products manufactured using the innovative and High -Tech manufacturing process known as Form – Fill – Seal Technology.
fresher B.Pharm / M.Pharm / M.Sc/B.SC; To perform IPQA, APQR, Market Complaints activities. Review of BMR, BPR, CAPA, QMS, OOS. Can handle instrument i.e HPLC- Dissolution.GC, IR.UV, QC QMS, Material testing. Candidates must be open to work in shift duties and having pharma experience in regulated plant like USFDA, MHRA should apply.
A Scientific Professional with Bachelor, Masters degree in Pharmacy, Life Sciences, Chemistry, Biological Sciences with a business management degree, MBA is preferred. A minimum of 9 years experience with at least 5 years in a technical field analytical background and at least 4 year of experience in a customer facing role.
Co-ordination with product development team to keep track of various projects. Sample seeding from suppliers for project initiation. Co-ordination with supplier, principle for arranging quality documents.
Ensure outcomes of variations are communicated in timely manner and databases/lists are up to date at all times, in accordance with agreed procedure as applicable
2-7 years of experience in production planning, change control, line clearance, deviation handling, autoclave operation TS and component, aseptic and control area operation, documentation, both SVP and LVP manufacturing etc.