Quality Control Officer
2 days ago
Lagos, Lagos State, Nigeria
Shalina Healthcare
Full-time
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About Shalina Healthcare:
Shalina Healthcare is one of the largest pharmaceutical companies in sub-Saharan Africa. For the last 40 years we have made it our mission to provide quality medicines to those who need it the most. We manufacture and distribute branded prescription and over-the-counter pharmaceutical and consumer products, across a broad range of therapeutic groups, including anti-malarial, antibiotics, anti-inflammatory and nutrition. We have a track record few can match and our brands are among the most trusted in Africa.
We are proud of our history and have big ambitions for the future. Our vision for 2030 is to be the health champion of Sub-Saharan Africa. To achieve this, we are looking for the right people to join us and create a lasting impact not just within our company but on the communities we serve.
Everyone in our company has a crucial role to play, and we are looking for people who identify with our Core Values and are as passionate about our Mission as we are.
The Global Supply Organization is a multi-continental Function that comprises of the entire Value Chain from product conceptualization to delivery to the commercial front. Within the Global Supply Organization are included, Research & Development, Project Management, Manufacturing, Quality, Supply Chain Management and Logistics.
Role: Quality Control Office
rDesignation: Office
rBase
location:
Lagos, Nigeri a Job Descriptio n:Analysis of FG/ RM/PM/IP/stability/validation/Water/hold time study & other analysis related in Quality control dep t.
Maintain, Monitor &Implementation of cGLP & cGMP as per latest norm s.
Sampling and analysis of incoming Raw materials, packaging materials and miscellaneous material s.
Calibration of Equipment’s / Instruments as per calibration schedule and monitoring of temperature-controlled equipmen t.
Destruction of respective records & QC Samples like Raw materials reference samples, & RM /PM/IP/FG/stability/Water/hold time study left over sample s.
Preparation of SOPs, Protocol and report for QC project s.
Reporting of OOS, OOT, deviations, change control Laboratory Incidence during analysis activit y.
Analysis and reporting of process validation samples, customer complaint, vendor samples and investigational sample s.
Inputting the quality reports, Data / Results entry of SFG, FG Raw material/Packaging materials in SAP syste m.
To comply with Internal and External Audit Observation s.
Preparation of volumetric solutions and reagents, Maintaining stock of chemicals and glassware s.
Preparation of working standard s.
To follow and maintain Good Chromatographic Practice s.
Preparation and maintenance of Analytical data sheets and Excel spread sheet s.
To maintain the housekeeping within the Laborator y.
Ensure and perform trend analysis of SFG and FG Qualificati ons4+ years of experience in a pharmaceutical Quality Control laborato ry.
Bachelor's Degree in Pharmacy, Chemistry, Biochemistry, Microbiology, Industrial Chemistry, or related Life Sciences discipli ne. Key Sk illsQuality Control Tes tingLaboratory Documentation & Data Integ ritycGLP & cGMP Compli anceAnalytical Instruments (HPLC/UV/Dissolut ion)SAP/Data E ntryOOS/OOT Investigation Sup portAttention to De tailTeamwork & Communica tion
location:
Lagos, Nigeri a Job Descriptio n:Analysis of FG/ RM/PM/IP/stability/validation/Water/hold time study & other analysis related in Quality control dep t.
Maintain, Monitor &Implementation of cGLP & cGMP as per latest norm s.
Sampling and analysis of incoming Raw materials, packaging materials and miscellaneous material s.
Calibration of Equipment’s / Instruments as per calibration schedule and monitoring of temperature-controlled equipmen t.
Destruction of respective records & QC Samples like Raw materials reference samples, & RM /PM/IP/FG/stability/Water/hold time study left over sample s.
Preparation of SOPs, Protocol and report for QC project s.
Reporting of OOS, OOT, deviations, change control Laboratory Incidence during analysis activit y.
Analysis and reporting of process validation samples, customer complaint, vendor samples and investigational sample s.
Inputting the quality reports, Data / Results entry of SFG, FG Raw material/Packaging materials in SAP syste m.
To comply with Internal and External Audit Observation s.
Preparation of volumetric solutions and reagents, Maintaining stock of chemicals and glassware s.
Preparation of working standard s.
To follow and maintain Good Chromatographic Practice s.
Preparation and maintenance of Analytical data sheets and Excel spread sheet s.
To maintain the housekeeping within the Laborator y.
Ensure and perform trend analysis of SFG and FG Qualificati ons4+ years of experience in a pharmaceutical Quality Control laborato ry.
Bachelor's Degree in Pharmacy, Chemistry, Biochemistry, Microbiology, Industrial Chemistry, or related Life Sciences discipli ne. Key Sk illsQuality Control Tes tingLaboratory Documentation & Data Integ ritycGLP & cGMP Compli anceAnalytical Instruments (HPLC/UV/Dissolut ion)SAP/Data E ntryOOS/OOT Investigation Sup portAttention to De tailTeamwork & Communica tion