Top Benefits
About the role
Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products.
From our world-class sites in North America and Asia, we deliver drug products with unparalleled quality to more than 100 markets around the world. Bora’s teams, technologies, and facilities work seamlessly together to enable our clients to deliver much-needed therapeutics to patients worldwide.
At Bora Pharmaceuticals, we see it as our mission, our duty, our responsibility, to make our success and our customer’s success more certain.
Why join Bora?
- Competitive salary
- A modern and state-of-the-art facility
- An on-site cafeteria with dedicated chefs
- On-site gym and basketball court
Click here for a video tour of our Mississauga facility: https://lnkd.in/evhPktDN
POSITION DESCRIPTION
JOB TITLE: QC Chemist
DEPARTMENT: Quality Control
POSITION REPORTING TO : QC Supervisors in Chemistry (Incoming Goods)
EMPLOYMENT TYPE: Permanent Full-Time
General Description:
Perform chemical analyses on Incoming Goods in accordance with local analytical methods or pharmacopeial monographs.
Responsibilities:
- Utilize analytical expertise in chemical and instrumental analysis (e.g. HPLC, GC, UV, IR) and wet chemistry measurement techniques.
- Work collaboratively with team members to collectively deliver quality results of the highest accuracy and precision.
- Maintain data integrity (ALCOA) and working with integrity.
- Be an active agent for continuous improvement in Quality control.
- Follow all safety policies, maintain a clean and orderly work area, and report any potentially unsafe conditions within the workplace.
- Maintain laboratory systems and participate in projects as required.
- Assist in investigations of OOS and OOT results.
- May be required to approve packaging component specifications.
- May be required to review and release products, raw materials & packaging components.
Qualifications:
Experience and Skills
- 1-2 years of quality Control experience in pharmaceutical laboratory environment or TIPT or equivalent diploma.
- Good theoretical and practical knowledge of instrumental techniques and demonstrated computer proficiency in LIMs software (e.g., Labware), Empower, MS Word and MS Excel.
- Demonstrated proficiency in basic analytical techniques.
- Good knowledge of laboratory GMP and the Pharmacopoeias.
Education
Required:
- College Diploma in Chemistry or a related science
- Computer proficiency for MS Word & MS Excel
- GMP experience/knowledge
Preferred:
- University degree in Chemistry
Working Conditions:
- Working within the chemistry laboratories.
- Working on the chemistry bench using chemicals and analytical equipment.
- 37.5-hour work week.
Bora is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals to apply to our career opportunities. Bora is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us at accessibility@bora-corp.com. Please do not send resumes to this e-mail and instead apply through the online application process of this posting.
About Bora Pharmaceuticals
Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in complex oral solid dose, liquids, semi-solids, ophthalmics and nasal sprays for pharmaceutical products. We operate from early phase clinical right through to commercial manufacturing with full packaging capabilities. From cell-line development and formulation to analytical services, clinical cGMP manufacturing and sterile fill/finish services, Bora now provides tailored development and manufacturing services to biologics developers. Bora owns and operates in ten state-of-the-art CGMP manufacturing facilities across Asia and North America – delivering to more than 100 markets around the world. Our sites have the highest international standards for manufacturing, packaging, R&D and analytical testing.
As a future focused CDMO, we know better than most that our own success is shaped by our partners victories. That's why, when you choose Bora - we make success more certain by following Bora’s 5Ps – Promises, Partnerships, Pride, People, and Progress. These 5 principles are Bora’s Pledge to our customers.
Follow us to find out more and keep up to date with Bora Pharmaceuticals.
Top Benefits
About the role
Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products.
From our world-class sites in North America and Asia, we deliver drug products with unparalleled quality to more than 100 markets around the world. Bora’s teams, technologies, and facilities work seamlessly together to enable our clients to deliver much-needed therapeutics to patients worldwide.
At Bora Pharmaceuticals, we see it as our mission, our duty, our responsibility, to make our success and our customer’s success more certain.
Why join Bora?
- Competitive salary
- A modern and state-of-the-art facility
- An on-site cafeteria with dedicated chefs
- On-site gym and basketball court
Click here for a video tour of our Mississauga facility: https://lnkd.in/evhPktDN
POSITION DESCRIPTION
JOB TITLE: QC Chemist
DEPARTMENT: Quality Control
POSITION REPORTING TO : QC Supervisors in Chemistry (Incoming Goods)
EMPLOYMENT TYPE: Permanent Full-Time
General Description:
Perform chemical analyses on Incoming Goods in accordance with local analytical methods or pharmacopeial monographs.
Responsibilities:
- Utilize analytical expertise in chemical and instrumental analysis (e.g. HPLC, GC, UV, IR) and wet chemistry measurement techniques.
- Work collaboratively with team members to collectively deliver quality results of the highest accuracy and precision.
- Maintain data integrity (ALCOA) and working with integrity.
- Be an active agent for continuous improvement in Quality control.
- Follow all safety policies, maintain a clean and orderly work area, and report any potentially unsafe conditions within the workplace.
- Maintain laboratory systems and participate in projects as required.
- Assist in investigations of OOS and OOT results.
- May be required to approve packaging component specifications.
- May be required to review and release products, raw materials & packaging components.
Qualifications:
Experience and Skills
- 1-2 years of quality Control experience in pharmaceutical laboratory environment or TIPT or equivalent diploma.
- Good theoretical and practical knowledge of instrumental techniques and demonstrated computer proficiency in LIMs software (e.g., Labware), Empower, MS Word and MS Excel.
- Demonstrated proficiency in basic analytical techniques.
- Good knowledge of laboratory GMP and the Pharmacopoeias.
Education
Required:
- College Diploma in Chemistry or a related science
- Computer proficiency for MS Word & MS Excel
- GMP experience/knowledge
Preferred:
- University degree in Chemistry
Working Conditions:
- Working within the chemistry laboratories.
- Working on the chemistry bench using chemicals and analytical equipment.
- 37.5-hour work week.
Bora is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals to apply to our career opportunities. Bora is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us at accessibility@bora-corp.com. Please do not send resumes to this e-mail and instead apply through the online application process of this posting.
About Bora Pharmaceuticals
Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in complex oral solid dose, liquids, semi-solids, ophthalmics and nasal sprays for pharmaceutical products. We operate from early phase clinical right through to commercial manufacturing with full packaging capabilities. From cell-line development and formulation to analytical services, clinical cGMP manufacturing and sterile fill/finish services, Bora now provides tailored development and manufacturing services to biologics developers. Bora owns and operates in ten state-of-the-art CGMP manufacturing facilities across Asia and North America – delivering to more than 100 markets around the world. Our sites have the highest international standards for manufacturing, packaging, R&D and analytical testing.
As a future focused CDMO, we know better than most that our own success is shaped by our partners victories. That's why, when you choose Bora - we make success more certain by following Bora’s 5Ps – Promises, Partnerships, Pride, People, and Progress. These 5 principles are Bora’s Pledge to our customers.
Follow us to find out more and keep up to date with Bora Pharmaceuticals.