Unicure Pharma, a leading name in the pharmaceutical industry, is thrilled to announce several exciting career opportunities for skilled and dedicated professionals. We are currently seeking individuals with a passion for quality and a commitment to excellence to join our growing team. Whether you’re an experienced professional or an ambitious recent graduate, we invite you to explore the positions detailed below and consider a rewarding career with Unicure Pharma.
Current Openings:
We are actively recruiting for the following roles:
QA Officers (Male)
Two positions available:
- Position 1: Focus on Documentation
- Experience: 1 to 5 years of experience in a QA role within the pharmaceutical industry.
- Expertise: Proficient in creating, reviewing, and maintaining comprehensive quality documentation, including batch records, deviation reports, and change controls. Strong understanding of cGMP (Current Good Manufacturing Practices) is essential. Experience with electronic document management systems (EDMS) is a plus. Excellent attention to detail and organizational skills are critical.
- Responsibilities: This role will primarily focus on ensuring the accuracy and completeness of all quality documentation related to manufacturing processes. You will work closely with other departments to ensure compliance with regulatory requirements.
- Position 2: Documentation & Shop Floor Activities
- Experience: 1 to 5 years of experience in a QA role within a pharmaceutical manufacturing environment.
- Expertise: In addition to the documentation skills listed above, experience with shop floor activities, including real-time quality checks, process monitoring, and problem-solving, is required. Knowledge of manufacturing processes and equipment is essential. Strong communication and interpersonal skills are critical for effective collaboration with shop floor personnel.
- Responsibilities: This role encompasses the responsibilities of Position 1, along with direct participation in shop floor quality control activities. You will monitor processes, identify potential quality issues, and work to resolve them proactively.
Key Skills for Both QA Officer Positions:
- Strong understanding of cGMP (Current Good Manufacturing Practices)
- Excellent documentation and record-keeping skills
- Proficiency in Microsoft Office Suite
- Strong attention to detail and accuracy
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
Officer – Engineering (Preventive Maintenance)
- Experience: 2 to 10 years of experience in preventive maintenance of pharmaceutical machinery.
- Expertise: Deep understanding of pharmaceutical manufacturing equipment and processes. Experience with troubleshooting, repairing, and maintaining various types of pharmaceutical machinery. Knowledge of relevant safety regulations and procedures. Proficiency in preventative maintenance scheduling and execution. Excellent problem-solving and analytical skills are required.
- Responsibilities: This crucial role involves planning, scheduling, and performing preventative maintenance on all pharmaceutical manufacturing equipment to ensure optimal performance and minimize downtime. You will also troubleshoot and repair equipment malfunctions and maintain detailed records of all maintenance activities.
QC Officers (Male/Female)
Two positions available:
- Position 1: Instrumentation Analysis (HPLC, GC, FTIR)
- Experience: 1 to 5 years of experience in a QC laboratory setting, with hands-on experience in analytical instrumentation.
- Expertise: Proficiency in operating and maintaining HPLC (High-Performance Liquid Chromatography), GC (Gas Chromatography), and FTIR (Fourier-Transform Infrared Spectroscopy) instruments. Experience with method validation and troubleshooting. Strong understanding of analytical chemistry principles and data analysis. Excellent laboratory techniques and adherence to safety protocols are essential.
- Responsibilities: This role will involve performing routine and non-routine analytical testing using various instrumentation to ensure the quality and purity of raw materials and finished products.
- Position 2: QC Documentation
- Experience: 1 to 5 years of experience in a QC laboratory setting, with a focus on documentation.
- Expertise: Proficiency in creating, reviewing, and maintaining comprehensive quality documentation, including test results, certificates of analysis, and deviation reports. Strong understanding of cGMP (Current Good Manufacturing Practices) is essential. Experience with electronic data management systems (EDMS) is a plus. Excellent attention to detail and organizational skills are critical.
- Responsibilities: This role will focus on ensuring the accuracy and completeness of all quality documentation related to testing and analysis within the QC laboratory. You will work closely with other team members to maintain accurate records and ensure compliance with regulatory requirements.
Why Choose Unicure Pharma?
Unicure Pharma offers a dynamic and rewarding work environment, with opportunities for professional growth and development. We are committed to providing our employees with a supportive and collaborative atmosphere. We offer a competitive salary and benefits package.
How to Apply:
Interested candidates are encouraged to submit their CVs and cover letters to: hr@unicurepharma.com
Visit our website for more information: www.unicurepharma.com
