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The Materia Company Ltd in Malta is looking to recruit an R&D Analytical Manager to join their team on a full-time basis.
Job Role:
The R&D Analytical Manager (AM) has the responsibility of leading analytical development and providing analytical solutions in support of the R&D projects. The AM shall provide guidance and participate directly in analytical method development, method validation, finished good testing, and stability of drug products. The incumbent is also accountable for overseeing the scientific rigor and quality of analytical work by contract labs and contract manufacturers. The AM will provide technical expertise to assist the R&D formulator during the product development process.
Job Tasks and Responsibilities:
Provide technical expertise in developing test strategy, analytical method development, and analytical method optimization for the developed products,
Manages the analytical function of the R&D lab,
Oversees analytical techniques, interpretations of analytical data, problem-solving, and troubleshooting as required for R&D approval,
Provide technical support to the Formulation Department & collaborate with the Project Manager in scoping special project work; aligning with the development team and executing projects,
Support formulation manager in the deployment of department strategies including exploring new techniques for smart testing and productivity,
Effectively and independently manage priorities and workflow of projects,
Deliver results within specified project timelines,
Draft, review, and/or approve analytical validation protocols and reports,
Manage analytical systems and ensure accurate analytical method development reporting,
Communicate results and findings amongst the development team,
Following up on developments and pending issues,
Draft and maintain SOPs related to analytical equipment and procedures,
Support digitization of database and research findings,
Identifies departmental needs and assists with recruits/hires/promote personnel as appropriate,
Develops staff through coaching, training, and other relevant experiences.
Education and Experience:
BSc, MSc in Biochemistry, Chemistry, Organic Chemistry, or a related science degree.
A minimum of 5 years experience in a pharmaceutical Analytical R&D laboratory / QC laboratory is mandatory.
Method development validation experience gained in an R&D environment would be preferable.
Knowledge of principles referring to QbD, GMP, GLP, and ICH Guidelines is considered an asset.
Possessing basic knowledge of applicable drug regulations as per ICH guidelines is considered an asset.
Ability to utilize Microsoft Word and Excel proficiently.
Key Competencies:
Critical thinking, great flexibility, and ability to multi-task dependent on the types of work that the department supports.
Excellent written and oral communication skills in English
Good Time management
Project management
Problem solving and troubleshooting
Self-motivated and results-driven; leadership skills and demonstrated teamwork and supervisory experience
Capable of learning and applying various analytical techniques
Experienced with statistical tools.
R&D Culture:
Our R&D team recognizes the potential and talent of our people are key to the success of the company. We share a set of beliefs that elevates our ability to reach our goals and business objectives. We encourage each other to pursue innovative solutions without fear of failure by nurturing a culture where talent development and continuous learning are the main priorities. We are a small team that works collaboratively to deliver meaningful outcomes.
*This is a rewarding opportunity for personal and professional growth. The AM will have a unique opportunity to expand his/her knowledge to help and sustain developed products.
The Materia Company Ltd in Malta is looking to recruit an R&D Analytical Manager to join their team on a full-time basis.
Job Role:
The R&D Analytical Manager (AM) has the responsibility of leading analytical development and providing analytical solutions in support of the R&D projects. The AM shall provide guidance and participate directly in analytical method development, method validation, finished good testing, and stability of drug products. The incumbent is also accountable for overseeing the scientific rigor and quality of analytical work by contract labs and contract manufacturers. The AM will provide technical expertise to assist the R&D formulator during the product development process.
Job Tasks and Responsibilities:
Provide technical expertise in developing test strategy, analytical method development, and analytical method optimization for the developed products,
Manages the analytical function of the R&D lab,
Oversees analytical techniques, interpretations of analytical data, problem-solving, and troubleshooting as required for R&D approval,
Provide technical support to the Formulation Department & collaborate with the Project Manager in scoping special project work; aligning with the development team and executing projects,
Support formulation manager in the deployment of department strategies including exploring new techniques for smart testing and productivity,
Effectively and independently manage priorities and workflow of projects,
Deliver results within specified project timelines,
Draft, review, and/or approve analytical validation protocols and reports,
Manage analytical systems and ensure accurate analytical method development reporting,
Communicate results and findings amongst the development team,
Following up on developments and pending issues,
Draft and maintain SOPs related to analytical equipment and procedures,
Support digitization of database and research findings,
Identifies departmental needs and assists with recruits/hires/promote personnel as appropriate,
Develops staff through coaching, training, and other relevant experiences.
Education and Experience:
BSc, MSc in Biochemistry, Chemistry, Organic Chemistry, or a related science degree.
A minimum of 5 years experience in a pharmaceutical Analytical R&D laboratory / QC laboratory is mandatory.
Method development validation experience gained in an R&D environment would be preferable.
Knowledge of principles referring to QbD, GMP, GLP, and ICH Guidelines is considered an asset.
Possessing basic knowledge of applicable drug regulations as per ICH guidelines is considered an asset.
Ability to utilize Microsoft Word and Excel proficiently.
Key Competencies:
Critical thinking, great flexibility, and ability to multi-task dependent on the types of work that the department supports.
Excellent written and oral communication skills in English
Good Time management
Project management
Problem solving and troubleshooting
Self-motivated and results-driven; leadership skills and demonstrated teamwork and supervisory experience
Capable of learning and applying various analytical techniques
Experienced with statistical tools.
R&D Culture:
Our R&D team recognizes the potential and talent of our people are key to the success of the company. We share a set of beliefs that elevates our ability to reach our goals and business objectives. We encourage each other to pursue innovative solutions without fear of failure by nurturing a culture where talent development and continuous learning are the main priorities. We are a small team that works collaboratively to deliver meaningful outcomes.
*This is a rewarding opportunity for personal and professional growth. The AM will have a unique opportunity to expand his/her knowledge to help and sustain developed products.