Quality Control Analyst will be part of the highly qualified QC team in a fast-paced environment, continuously challenging performance in regards to quality standards, systems and operating procedures.

Joining our Organization, you will recognize that:

• Our company fosters a supportive and collaborative work environment and promotes work-life balance.
• We offer Career Development and Growth Opportunities investing in  training and development programs
• Challenging and Meaningful Work for Employees motivated by purpose-driven work
• Competitive Compensation and Benefits: Fair and competitive compensation packages, including salary, bonuses, and benefits, are essential in attracting top talent.
• Company Reputation and Stability: We are a company with a track record of success, a strong reputation,a good market position and financial stability, positive reviews from current and former employees.
• Career paths aren't predefined and you have the opportunity to grow, learn from our industry experts, and develop the way you want to.

Job Description

 Ensure that lab cleanliness and safety standards are maintained. Develop and qualify new testing methods.

Train other analysts to perform laboratory procedures and assays. Participate in internal and external audits as required.

Identify and troubleshoot equipment problems.

Evaluate new technologies and methods to make recommendations regarding their use.

Serve as a technical liaison between quality control and other departments, vendors, or contractors. Write technical reports or documentation such as deviation reports, testing protocols, and trend analyses. Write or revise standard quality control operating procedures.

Supply quality control data necessary for regulatory submissions. Receive and inspect raw materials.

Review data from contract laboratories to ensure accuracy and regulatory compliance.

Prepare or review required method transfer documentation including technical transfer protocols or reports. Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines. Participate in out-of-specification and failure investigations and recommend corrective actions.

Interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data for release.

Identify quality problems and recommend solutions.

Evaluate analytical methods and procedures to determine how they might be improved.

Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms.

Calibrate, validate, or maintain laboratory equipment.

Compile laboratory test data and perform appropriate analyses.

Conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples.

Requirements

• Bachelor’s degree (Chemistry)
• Postgraduate degree is desirable
• 1+ year of related pharmaceutical laboratory experience in a cGMP environment
• Prior experience in method development/validation and/or transfer/verification, protocols, and troubleshooting
• Fluency in English language written and oral

Being a member of our Organization you will have the opportunity to grow, learn from our industry experts and achieve your career aspirations.

We are investing in the development of our team, committed to meeting the needs of our employees and their families.

Our environment is geared to fuel curiosity, encourage experimentation, and generate learning as this is the way we develop ourselves and our organization.

With competitive compensation and recognition programs and standout benefits we ensure employees feel supported both at work and home.

We provide employees with a private insurance contract for their optimal health and well-being.