Open Vacancies at Sunny Pharmaceuticals Company
Validation Specialist –Sterile Pharmaceutical Manufacturing
Key Responsibilities:
Assist in preparing and executing calibration & Qualification plans.
Assist in preparing and executing validation protocols (IQ/OQ/PQ)
Support aseptic process simulations (media fills), cleaning validation, and documentation
Work closely with QA, Engineering, and Production teams
Qualifications:
Bachelor’s degree in Pharmacy or Science.
Familiarity with GMP and sterile manufacturing (internships/projects a plus)
Strong attention to detail and willingness to learn.
Experience from 0:2 year
interested candidates send CVs to : eali@sunnyph.com , mentioned the job title in the subject line.
Risk Assessment Section Head – Sterile Pharmaceutical Manufacturing
Key Responsibilities:
Lead all risk assessment activities related to sterile manufacturing processes and quality systems.
Apply tools like FMEA, HACCP, and Fault Tree Analysis to proactively identify and evaluate risks.
Collaborate with cross-functional teams to manage risk in investigations, deviations, CAPAs, and change controls.
Ensure documentation and assessments align with ICH Q9 and EU GMP Annex 1.
Train staff on risk management principles and regulatory best practices.
Support audits and inspections as the subject matter expert for risk assessment.
Develop and monitor KPIs related to risk identification, analysis, and mitigation effectiveness.
Qualification:
Bachelors in Pharmacy or Science.
Minimum of 8 years’ experience in sterile pharmaceutical manufacturing or quality assurance.
Deep understanding of aseptic processing, contamination control, and GMP compliance.
Strong analytical, communication, problem-solving, leadership skills documentation skills.
Proven experience leading cross-functional teams and facilitating risk-based decision-making.
Certification in risk management.
Interested candidates send CV to : eali@sunnyph.com , mentioned the job title in the subject line.
GMP & Compliance Senior – Sterile Pharmaceutical Manufacturing
Key Responsibilities
Monitor, assess, and ensure GMP compliance across sterile manufacturing, quality control, and support areas.
Lead internal audits, inspection readiness, and regulatory inspections.
Support deviation investigations, CAPAs, change controls, and risk assessments.
Provide GMP guidance to cross-functional teams and drive continuous quality improvement.
Maintain and improve quality systems in alignment with global best practices and data integrity requirements.
Review and approve GMP documents including SOPs, protocols, reports, and validation documentation.
Qualifications
Bachelors in Pharmacy or Science
0-2 years’ experience in GMP compliance in a sterile pharmaceutical
Deep knowledge of GMP guidelines (FDA, EMA, WHO), Annex 1, and data integrity standards
Strong communication, problem-solving, and auditing skills
Preferred Skills
Experience with regulatory inspections (FDA, EMA, etc.)
Lead auditor certification (ISO/GMP) is a plus
Interested candidates send CVs to : eali@sunnyph.com , mentioned the job title in the subject line.
Finished goods Storekeeper
Responsibilities:
– Receive finished products
– Prepare report of quantities of finished goods received from production and complete daily counts to verify the accuracy
– Maintain an accurate inventory of finished goods
Stock finished goods in assigned locations while adjusting locations as needed
– Organize the finished goods in the store according to the proper storage conditions of each
– Secure all the finished goods in the store
– Assure the security of the store
– Facilitate in loading and unloading trucks for prompt delivery and to assure proper amount and requested items are loaded.
Requirements:
– Previous experience of similar role is mandated preferably in Pharmaceutical Sector.
– Bsc degree
send CVs to : eali@sunnyph.com , mentioned the job title in the subject line.