- Merck & Co. (Boston, MA)
- …(including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs, and global clinical trials operations)Provide ... point in the drug development process, working closely with scientific, regulatory , statistical, and modelling colleagues across the organization to translate the… more
- Syner-G BioPharma Group (Boston, MA)
- …strategic partner for life science companies. We provide integrated regulatory and biopharmaceutical development services spanning early development to post-market, ... along with operational strategy and support. With a global team of 400 employees across North America and...phases of the drug development lifecycle, from discovery and regulatory approval to technology transfer and the support in… more
- Syner-G BioPharma Group (Boston, MA)
- …strategic partner for life science companies. We provide integrated regulatory and biopharmaceutical development services spanning early development to post-market, ... along with operational strategy and support. With a global team of 400 employees across North America and...phases of the drug development lifecycle, from discovery and regulatory approval to technology transfer and the support in… more
- Cipla (Fall River, MA)
- …complaints, supporting packaging, and packaging components within approved proceduresand regulatory requirements. The job duties for this position include but ... activities. Maintains documentation in accordance with internal procedures and regulatory requirements(ie, GMP, SOPs etc.). Follow strict internal protocols and… more
- Cipla (Fall River, MA)
- …on time, ensuring accuracy and completeness. Adhering to all cGMPs, compliance/ regulatory mandates and quality requirements. Complying with company policies and ... instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic… more
- Cipla (Fall River, MA)
- …operations for compliance to cGMP and set standards to meet the regulatory requirement and to ensure audit readiness. Ensure proper receipt, verification, ... instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic… more
- Cipla (Fall River, MA)
- …part of a team. Capable of handling and participating in compliance and regulatory audits at the local and federal levels. Experience in Inhalation products (Metered ... required. Safety/Personal Protective Equipment (PPE) required for this job. GLOBAL COMPANY: Cipla is a leading global ...believes that our biggest assets are the employees who lead us to prosperity and growth in the future.… more
- Cipla (Fall River, MA)
- …of API equipment and products in compliance with site SOPs and regulatory guidance. Autonomously leads and manages projects to implement continuous improvement ... opportunities. Lead and/or support root cause investigations related to performance...Defends the validation programs and strategies to customers and regulatory auditors. Performs weekly quality reviews of Master Control… more
- Cipla (Fall River, MA)
- …AM - 5:00 PM (May vary based on business needs) Reports To : QA QMS Lead Salary Range : $64,272 - $77,662 PURPOSE The QA Document Control Associate in a ... controlled documents to ensure compliance with GMP, GDP, and regulatory standards such as FDA 21 CFR Part 11,...Quality Team. The position reports to the QA QMS Lead and may be matrixed to other functional leaders… more
- Cipla (Fall River, MA)
- …validation of equipment and products in compliance with site SOPs and regulatory guidance. Provides data to support management evaluation of performance trends. Owns ... leads and manages projects to implement continuous improvement opportunities. Lead and/or support root cause investigations related to performance trends… more
- Cipla (Fall River, MA)
- …posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's US Subsidiaries or Affiliates. ... About Cipla Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals… more
- Cipla (Fall River, MA)
- …instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic ... which include hooded or full face supplied air respirators. GLOBAL COMPANY Cipla is a leading global ...believes that our biggest assets are the employees, who lead us to prosperity and growth in the future.… more
- Cipla (Fall River, MA)
- …instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic ... (SAR), which include hooded or full face supplied air respirators. GLOBAL COMPANY Cipla is a leading global ...believes that our biggest assets are the employees, who lead us to prosperity and growth in the future.… more
- Cipla (Fall River, MA)
- …instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic ... which include hooded or full face supplied air respirators. GLOBAL COMPANY Cipla is a leading global ...believes that our biggest assets are the employees, who lead us to prosperity and growth in the future.… more
- Cipla (Fall River, MA)
- …Verifying process validation and characterization-related documents. Coordinating with the Regulatory Affairs (RA) and Analytical Laboratory Teams to arrange ... analysis. Capable of supporting and participating in compliance and regulatory audits at the local and federal levels. Experience...may be requested or required based on business needs. GLOBAL COMPANY Cipla is a leading global … more
- Cipla (Fall River, MA)
- …on time, ensuring accuracy and completeness. Adhering to all cGMPs, compliance/ regulatory mandates and quality requirements. Complying with company policies and ... instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic… more
- Cipla (Fall River, MA)
- …on time, ensuring accuracy and completeness. Adhering to all cGMPs, compliance/ regulatory mandates and quality requirements. Complying with company policies and ... instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic… more
- Cipla (Fall River, MA)
- …cause identification and analysis. Capable of handling and participating in compliance and regulatory audits at the local and federal levels. Must be proficient in ... which include hooded or full face supplied air respirators. GLOBAL COMPANY Cipla is a leading global ...believes that our biggest assets are the employees who lead us to prosperity and growth in the future.… more
- Parexel (Boston, MA)
- …development of appropriate responses. - Participate in Safety Management Team (SMT) and Global Regulatory Team (GRT) meetings to provide expert input on ... tracked, and delivered. **Key Responsibilities:** - Serve as the global labelling lead for multiple products, providing...the idea of being a key player in a global regulatory role - apply today! \#LI-LB1… more
- Lundbeck (Boston, MA)
- …that values being curious, adaptable, and accountable? Lundbeck is a global biopharmaceutical company focusing exclusively on brain health. With more than ... in the primary care and neurology settings. As an Account Manager, you lead the promotion of our psychiatry portfolio, executing sales and marketing strategies with… more
