Chemist, Analytical

Sun Pharmaceutical Industries, Inc.; Brampton; On-site; CAD 64,000 - 80,000; Full time

Job summary

Sun Pharmaceuticals Industries, Inc. in Brampton, Canada, seeks a scientist to conduct analytical development and research to support new product development, under supervision.

The role includes method development, validation, and testing of marketed and prototype products to meet timelines. Responsibilities include GC/HPLC testing, method validation, documentation, and contributing to product approvals while maintaining GMP/GLP standards.

Qualifications

• B. Sc. in Chemistry or related discipline and experience in a pharmaceutical-related field.
• In-depth knowledge of gas and liquid chromatography, spectroscopy and other analytical techniques employed in the pharmaceutical development.
• Familiarity with modern computer assisted analytical instrumentation methods and with older techniques (i.e. titration).
• Experience with method validation and development activities.
• Good knowledge and understanding of GMP-s and GLP-s, as well as with pertinent FDA and Health Canada guidelines.
• Ability to clearly communicate and work effectively in a team-based environment.
• Regular problem solving with significant degree of judgment coupled with excellent logical skills required. Problems typically include chemistry related issues (i.e. understanding the chemistry/degradation of the active), instrumentation related problems.

Responsibilities

• Perform testing using GC/HPLC techniques as well as specialized testing using particle size analysis, in‑vitro, spectroscopic analysis and other techniques as required.
• Perform development/validation of new analytical methods (with guidance from senior R&D staff).
• Prepare method development, validation and other research reports.
• Perform release of R&D products and raw materials.
• Participate in activities leading to product approval under the guidance of Senior R&D staff (e.g. deficiency letter responses for chemistry issues, investigations, etc.).
• Assist with laboratory investigation activities.
• Report and clearly document all research work performed.
• Report GMP work in accordance with current GMP/GLP regulations.
• Initiate and follow through with actions required for change controls.
• Maintain a clean laboratory environment and ensure that safety regulations are followed.
• Complete all training assignments and maintain personal training records.
• Flexibility to work shift schedules when required.
• Other duties as assigned.

Skills

Gas chromatography

Liquid chromatography

Spectroscopy

Analytical techniques

Data analysis

Education

B. Sc. in Chemistry

Tools

GC/HPLC instruments

Job description

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Driven by abold pursuit of scienceand fueled byan unwavering commitment to patients, Sun Pharma is a leading global pharmaceutical company, providing high-quality medicines trusted by healthcare professionals and patients.

As part of our mission toReach People and Touch Lives, we deliverInnovative Medicines, Generics and Consumer Healthcare productsthat improve the lives of millions of people. With a broadly diversified portfolio of products that span multiple therapeutic areas, weimprove access to effective, affordable treatmentsthat promote better health and well-being.

Reaching People. Touching Lives.

Job purpose

The main responsibilities of this position are to conduct analytical development and research to support development of new products. This work is conducted under supervision of the Supervisor and includes method development, validation, as well as testing marketed and prototype products required for product development. Work is completed in a timely manner ensuring departmental and corporate goals are being met.

Duties and responsibilities

• Perform testing using advanced GC/HPLC techniques as well as specialized testing using particle size analysis, in‑vitro, spectroscopic analysis and other techniques as required


• Perform development /validation of new analytical methods (with guidance from senior R&D staff)


• Prepare method development, validation and other research reports.


• Perform release of R&D products and raw materials


• Participate in activities leading to product approval under the guidance of Senior R&D staff (ie. deficiency letter responses for chemistry issues, investigations, etc.)


• Assist with laboratory investigation activities


• Report and clearly document all research work performed


• Report GMP work in accordance with current GMP/GLP regulations


• Initiate and follow through with actions required for change controls


• Maintain a clean laboratory environment and ensure that safety regulations are followed


• Complete all training assignment and maintain personal training records.


• Flexibility to work shift schedules when required


• Other duties as assigned

Additional responsibility (Only applicable to customer facing roles)

Report any adverse event received from customers for company products to the pharmacovigilance department / Drug Safety on the same day or within 1 business day

Qualifications

• B. Sc. in Chemistry or related discipline and experience in a pharmaceutical-related field


• In-depth knowledge of gas and liquid chromatography, spectroscopy and other analytical techniques employed in the pharmaceutical development


• Familiarity with modern computer assisted analytical instrumentation methods and with older techniques (i.e. titration)


• Experience with method validation and development activities


• Good knowledge and understanding of GMP-s and GLP-s, as well as with pertinent FDA and Health Canada guidelines


• Ability to clearly communicate and work effectively in a team-based environment


• Regular problem solving with significant degree of judgment coupled with excellent logical skills required. Problems typically include chemistry related issues (i.e. understanding the chemistry/degradation of the active), instrumentation related problems.

Working conditions

Generally, fairly pleasant surroundings. Occasional exposure to higher than normal noise levels. Frequent, daily exposure to various chemicals used in the testing of raw materials, components and finished products. Occasional exposure to unpleasant odors resulting from testing procedures. Fairly level temperatures. Mixture of standing and walking, some light lifting and/or movement of material/ instruments.

Physical requirements

Office based role

Direct reports

NA

This posting is for an existing vacancy.

The presently‑anticipated base compensation pay range for this position is $64,000 to $80,000. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; RRSP savings plan; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.

The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.

The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).

We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, ethnic origin, citizenship, ancestry, sex, age, marital status, family status, physical or mental disability, gender identity, gender expression or any other ground protected by applicable human rights legislation.

The Company uses artificial intelligence to screen, assess or select applicants.

Notice to Agency and Search Firm Representatives: Sun Pharmaceuticals Industries, Inc. (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Sun employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Sun. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.