The Technical Writer position is responsible for writing methods protocols reports SOPs and evaluating compendia procedures as it impacts the pharmaceutical products or raw materials.
- Manage medium and larger size projects and in collaboration with client and internal resources.
- Work with department manager and schedule projects according to projects prioritization and work with groups and functions to manage resources efficiently.
- Leading technical writer team for improvement initiatives and workload distribution.
- Responsible for supporting the scientists in R&D to prepare the documentation as required by clients including follow up of change controls maintaining the templates for laboratory documents.
- In addition responsible for periodic review of the compendia changes and providing evaluation as it impacts the Raw Material Finished Product and R&D groups within Analytical Operations.
- Working with chemistry laboratory personnel write or review reports for method development feasibility transfer verification and validation projects.
- Working with chemistry laboratory personnel write or review client methods for routine sample analysis as needed.
- Review various lab documents.
- Ensure timely review of compendia updates such as USP EP JP.
- Document and communicate the compendia changes to impacted departments.
Qualifications :
Bachelors Degree
Masters in Science
3 to 5 years experience in a laboratory setting with Min 2 years of Pharmceutical Technical Writing
Demonstrated work with cGMP
Proficient with lab software
Additional Information :
SGS is an Equal Opportunity Employer and as such we recruit hire train and promote persons in all job classifications without regard to race color religion sex national origin disability age marital status sexual orientation gender identity or expression and Indigenous status or any other characteristics protected by law.
To perform this job successfully an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge skills and/or abilities required.
This job description should not be construed as an exhaustive statement of duties responsibilities or requirements but a general description of the job. Nothing contained herein restricts the companys rights to assign or reassign duties and responsibilities to this job at any time.
Accommodations are available on request for qualified candidates during each stage of the recruitment process.
Please note that candidates applying for Canadian job openings should be authorized to work in Canada.
Remote Work :
No
Employment Type :
Contract
The Technical Writer position is responsible for writing methods protocols reports SOPs and evaluating compendia procedures as it impacts the pharmaceutical products or raw materials. Manage medium and larger size projects and in collaboration with client and internal resources.Work with department ...
The Technical Writer position is responsible for writing methods protocols reports SOPs and evaluating compendia procedures as it impacts the pharmaceutical products or raw materials.
- Manage medium and larger size projects and in collaboration with client and internal resources.
- Work with department manager and schedule projects according to projects prioritization and work with groups and functions to manage resources efficiently.
- Leading technical writer team for improvement initiatives and workload distribution.
- Responsible for supporting the scientists in R&D to prepare the documentation as required by clients including follow up of change controls maintaining the templates for laboratory documents.
- In addition responsible for periodic review of the compendia changes and providing evaluation as it impacts the Raw Material Finished Product and R&D groups within Analytical Operations.
- Working with chemistry laboratory personnel write or review reports for method development feasibility transfer verification and validation projects.
- Working with chemistry laboratory personnel write or review client methods for routine sample analysis as needed.
- Review various lab documents.
- Ensure timely review of compendia updates such as USP EP JP.
- Document and communicate the compendia changes to impacted departments.
Qualifications :
Bachelors Degree
Masters in Science
3 to 5 years experience in a laboratory setting with Min 2 years of Pharmceutical Technical Writing
Demonstrated work with cGMP
Proficient with lab software
Additional Information :
SGS is an Equal Opportunity Employer and as such we recruit hire train and promote persons in all job classifications without regard to race color religion sex national origin disability age marital status sexual orientation gender identity or expression and Indigenous status or any other characteristics protected by law.
To perform this job successfully an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge skills and/or abilities required.
This job description should not be construed as an exhaustive statement of duties responsibilities or requirements but a general description of the job. Nothing contained herein restricts the companys rights to assign or reassign duties and responsibilities to this job at any time.
Accommodations are available on request for qualified candidates during each stage of the recruitment process.
Please note that candidates applying for Canadian job openings should be authorized to work in Canada.
Remote Work :
No
Employment Type :
Contract
View more
View less