QC Chemist Associate
Unither Pharmaceuticals
Date: 15 hours ago
City: Rochester, NY
Contract type: Full time
Who we are?
We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients’ lives to as many people as possible.
With 30 years of technological expertise, we position ourselves as a world leader in sterile single dose with 10 sites on 4 continents and more than 2000 employees.
Since 2013, our site Unither Manufacturing LLC. based in Rochester (NY), specializes in the manufacture of Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 280 employees.
Your role
Reporting to the Lab Supervisor ,
JOB SUMMARY:
Performs routine analyses of materials, drug substances and drug products following cGMPs. May support analytical method development & validation, and analytical troubleshooting under technical supervision. Assists with maintaining lab quality systems.
ESSENTIAL DUTIES / RESPONSIBILITIES:
Completed Analyses (40%)
Performs, interprets, evaluates, and records routine and some non-routine analytical lab tests of materials, drug substances and drug products following CGMPs.
Execute protocols, experiments as written.
Maintains instruments and equipment. Sets up instruments and conducts sample tests. Performs routine calibration of instrumentation. Ensures an adequate supply of test materials are available to perform daily testing.
Maintains and updates training records in a timely manner.
Safe, Compliant, Efficient Labs (30%)
Supports lab systems as assigned and maintains laboratory in compliance with SOPs, cGMPs, HS&E requirements, and FDA, DEA, USP, EP, and OSHA regulations.
Problems Identified (30%)
Identifies and communicates actual and potential problems.
May support/provide input for investigations, troubleshooting, and method development/validation with supervision.
Writes basic investigations with supervision.
Your profile
REQUIRED EDUCATION: Associate’s Degree (Bachelor’s preferred) in Chemistry or related science
QUALIFICATIONS/EXPERIENCE:
A.A.S. with 2+ yrs. or B.S. with 0+ yrs. experience in chemistry or related science discipline.
SPECIFIC SKILLS:
Experience with laboratory analytical techniques preferred. Experience in a cGMP environment a plus.
Familiarity in 2 or more following areas: HPLC, GC, UV-VIS, FTIR, dissolution.
Experience in written notebook documentation practices a plus.
Write basic investigations with supervision.
Computer Skills:
Basic Outlook skills as evidenced by creating and sending messages, working with address books, message handling, creating and using personal folders, scheduling appointments, working with meeting requests and managing tasks.
Basic Microsoft Word skills as evidenced by the ability to produce basic business letters and simple tables and charts; as well as check spelling, set tabs, change page orientation, sort, save, open and organize electronic files.
Basic Excel skills as evidenced by the ability to use workbooks, create simple formulas, insert and delete data, create and edit charts, filter and sort lists, and format data.
Familiarity with LIMS and instrument operating software desirable.
PHYSICAL REQUIREMENTS/ENVIRONMENT: (List the details of the environment within/under which work is performed and physical requirements for this position.)
Must demonstrate visual acuity, color recognition, finger dexterity.
The ability to read, write and communicate in English.
Work responsibilities involve chemical and biological agents that have assigned biological and chemical hazards.
Sitting approximately 50% of day and standing approximately 50% of day.
Work responsibilities may involve repetitive use of the hands through keyboarding, simple grasping and fine manipulation.
Occasional lifting of up to 35 pounds.
Normal office environment and occasional controlled environment work that may require removal of jewelry and cosmetics.
Occasionally subjected to weekend, holiday and irregular hours.
Compensation Range
21.64 - 26.44 USD
We are a dynamic company driven by a spirit of victory and are therefore pursuing strong growth while maintaining a close relationship with our customers and employees.
Our culture is based on 5 values: Respect, Responsibility, Trust, Courage and Innovation. We are committed to bringing these values to life with our employees by granting them a high degree of autonomy in the exercise of their profession and by encouraging their initiatives.
We are committed to providing them with working conditions and atmosphere that is conducive to their development and the expression of their potential.
We propose you to integrate a site that values the meaning of work and that entrusts our employees with a high level of responsibility.
Join us and make a difference!
We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients’ lives to as many people as possible.
With 30 years of technological expertise, we position ourselves as a world leader in sterile single dose with 10 sites on 4 continents and more than 2000 employees.
Since 2013, our site Unither Manufacturing LLC. based in Rochester (NY), specializes in the manufacture of Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 280 employees.
Your role
Reporting to the Lab Supervisor ,
JOB SUMMARY:
Performs routine analyses of materials, drug substances and drug products following cGMPs. May support analytical method development & validation, and analytical troubleshooting under technical supervision. Assists with maintaining lab quality systems.
ESSENTIAL DUTIES / RESPONSIBILITIES:
Completed Analyses (40%)
Performs, interprets, evaluates, and records routine and some non-routine analytical lab tests of materials, drug substances and drug products following CGMPs.
Execute protocols, experiments as written.
Maintains instruments and equipment. Sets up instruments and conducts sample tests. Performs routine calibration of instrumentation. Ensures an adequate supply of test materials are available to perform daily testing.
Maintains and updates training records in a timely manner.
Safe, Compliant, Efficient Labs (30%)
Supports lab systems as assigned and maintains laboratory in compliance with SOPs, cGMPs, HS&E requirements, and FDA, DEA, USP, EP, and OSHA regulations.
Problems Identified (30%)
Identifies and communicates actual and potential problems.
May support/provide input for investigations, troubleshooting, and method development/validation with supervision.
Writes basic investigations with supervision.
Your profile
REQUIRED EDUCATION: Associate’s Degree (Bachelor’s preferred) in Chemistry or related science
QUALIFICATIONS/EXPERIENCE:
A.A.S. with 2+ yrs. or B.S. with 0+ yrs. experience in chemistry or related science discipline.
SPECIFIC SKILLS:
Experience with laboratory analytical techniques preferred. Experience in a cGMP environment a plus.
Familiarity in 2 or more following areas: HPLC, GC, UV-VIS, FTIR, dissolution.
Experience in written notebook documentation practices a plus.
Write basic investigations with supervision.
Computer Skills:
Basic Outlook skills as evidenced by creating and sending messages, working with address books, message handling, creating and using personal folders, scheduling appointments, working with meeting requests and managing tasks.
Basic Microsoft Word skills as evidenced by the ability to produce basic business letters and simple tables and charts; as well as check spelling, set tabs, change page orientation, sort, save, open and organize electronic files.
Basic Excel skills as evidenced by the ability to use workbooks, create simple formulas, insert and delete data, create and edit charts, filter and sort lists, and format data.
Familiarity with LIMS and instrument operating software desirable.
PHYSICAL REQUIREMENTS/ENVIRONMENT: (List the details of the environment within/under which work is performed and physical requirements for this position.)
Must demonstrate visual acuity, color recognition, finger dexterity.
The ability to read, write and communicate in English.
Work responsibilities involve chemical and biological agents that have assigned biological and chemical hazards.
Sitting approximately 50% of day and standing approximately 50% of day.
Work responsibilities may involve repetitive use of the hands through keyboarding, simple grasping and fine manipulation.
Occasional lifting of up to 35 pounds.
Normal office environment and occasional controlled environment work that may require removal of jewelry and cosmetics.
Occasionally subjected to weekend, holiday and irregular hours.
Compensation Range
21.64 - 26.44 USD
- The referenced compensation range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.
We are a dynamic company driven by a spirit of victory and are therefore pursuing strong growth while maintaining a close relationship with our customers and employees.
Our culture is based on 5 values: Respect, Responsibility, Trust, Courage and Innovation. We are committed to bringing these values to life with our employees by granting them a high degree of autonomy in the exercise of their profession and by encouraging their initiatives.
We are committed to providing them with working conditions and atmosphere that is conducive to their development and the expression of their potential.
We propose you to integrate a site that values the meaning of work and that entrusts our employees with a high level of responsibility.
Join us and make a difference!
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