Stage 4 Solutions
Regulatory Documentation Analyst Pharma (Hybrid New Brunswick, NJ)
Stage 4 Solutions, New Brunswick, New Jersey, us, 08933
Regulatory Documentation Analyst Pharma (Hybrid New Brunswick, NJ)
We are seeking a Documentation Analyst for a global pharmaceutical client. This position involves compiling information from scientists, authoring the chemistry, manufacturing, and controls (CMC) sections of regulatory documents, and performing data integrity checks to support the timely submissions of both investigational and marketing applications for small and large molecules.
This is a 40-hour per week, 6-month contract (extensions possible), 50% onsite role in New Brunswick, NJ.
This is a W2 role as a Stage 4 Solutions employee. Health benefits and 401K are offered.
Responsibilities:
Compiling information from scientists, authoring the chemistry, manufacturing, and controls (CMC) sections of regulatory documents, and performing data integrity checks to support the timely submissions of both investigational and marketing applications for small and large molecules. Constructive interactions with other members of a team to approach problem-solving. Requirements: 4+ years of experience in Regulatory Documentation and/or Authoring experience (not just formatting) in the Pharma industry. Knowledge of fundamental principles of organic chemistry, the critical evaluation of analytical data, and it is preferred to have experience in drug substance and/or drug product CMC development. Strong organic or Medicinal chemistry. Familiarity with computer-assisted document preparation tools is desirable. B.S. in Chemistry is required. An M.S. or Ph.D. in Organic or Medicinal Chemistry is strongly preferred. Please submit your resume to our network at Stage 4 Solutions Careers (please apply to the Regulatory Documentation Analyst Pharma (Hybrid New Brunswick, NJ) role.
Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.
Compensation: $38/hr. - $41.81/hr. Seniority level
Mid-Senior level Employment type
Full-time Job function
Administrative Business Consulting and Services
#J-18808-Ljbffr
We are seeking a Documentation Analyst for a global pharmaceutical client. This position involves compiling information from scientists, authoring the chemistry, manufacturing, and controls (CMC) sections of regulatory documents, and performing data integrity checks to support the timely submissions of both investigational and marketing applications for small and large molecules.
This is a 40-hour per week, 6-month contract (extensions possible), 50% onsite role in New Brunswick, NJ.
This is a W2 role as a Stage 4 Solutions employee. Health benefits and 401K are offered.
Responsibilities:
Compiling information from scientists, authoring the chemistry, manufacturing, and controls (CMC) sections of regulatory documents, and performing data integrity checks to support the timely submissions of both investigational and marketing applications for small and large molecules. Constructive interactions with other members of a team to approach problem-solving. Requirements: 4+ years of experience in Regulatory Documentation and/or Authoring experience (not just formatting) in the Pharma industry. Knowledge of fundamental principles of organic chemistry, the critical evaluation of analytical data, and it is preferred to have experience in drug substance and/or drug product CMC development. Strong organic or Medicinal chemistry. Familiarity with computer-assisted document preparation tools is desirable. B.S. in Chemistry is required. An M.S. or Ph.D. in Organic or Medicinal Chemistry is strongly preferred. Please submit your resume to our network at Stage 4 Solutions Careers (please apply to the Regulatory Documentation Analyst Pharma (Hybrid New Brunswick, NJ) role.
Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.
Compensation: $38/hr. - $41.81/hr. Seniority level
Mid-Senior level Employment type
Full-time Job function
Administrative Business Consulting and Services
#J-18808-Ljbffr