PharmaLex

HQ
Burlington, Massachusetts, USA
1,385 Total Employees
Year Founded: 1994

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Jobs at PharmaLex

Search the 10 jobs at PharmaLex

Recently posted jobs

Biotech • Pharmaceutical
The Process Development Scientist is responsible for conceiving, designing, and executing scientific experiments that aid in project completion. This role includes data analysis, ensuring compliance with protocols, developing new protocols, and authoring various scientific documents. The scientist will also collaborate with others, monitor scientific advancements in the field, and may lead department-wide initiatives.
22 Hours Ago
Juncos, PRI
Biotech • Pharmaceutical
The Quality Engineer I role involves developing and maintaining quality standards for software systems in a regulated environment. Responsibilities include conducting evaluations of software systems, ensuring compliance with documentation, collaborating with engineering teams, and implementing quality assurance tests and procedures.
22 Hours Ago
Ponce, PRI
Biotech • Pharmaceutical
The Process Engineer I will recommend and implement modifications to equipment and processes to enhance quality and efficiency. Responsibilities include conducting statistical analysis, ensuring compatibility between product designs and manufacturing processes, and developing manufacturing processes compliant with regulations. The role also involves troubleshooting and conducting root cause analysis.
22 Hours Ago
Makati, Southern Manila District, National Capital Region, PHL
Biotech • Pharmaceutical
The Junior Commercial Analyst supports the Senior Commercial Analyst by providing sales and marketing reporting and insights. They utilize CRM systems like Salesforce, PowerBI, and SQL-based systems to develop scalable reports and dashboards, identify performance trends, and maintain accurate data quality.
22 Hours Ago
Villalba, PRI
Biotech • Pharmaceutical
The Sr Supplier Qual Engineer is responsible for ensuring suppliers deliver quality parts and materials. They qualify suppliers, monitor parts through the manufacturing cycle, resolve supplier-related issues, and conduct regular audits to ensure compliance with GMP and quality standards. This role requires effective communication with suppliers and internal stakeholders, as well as providing feedback on supplier performance.
8 Days Ago
Juncos, PRI
Biotech • Pharmaceutical
The Data Scientist will lead advanced analytics projects to develop analytical models and insights, collaborating with various business partners to solve specific business problems and create business impact through strategic advanced analytics techniques.
9 Days Ago
Juncos, PRI
Biotech • Pharmaceutical
The Quality Engineer II develops and maintains quality standards and protocols for materials processing, collaborates with engineering and manufacturing to ensure standards are met, designs testing mechanisms, conducts quality tests, performs statistical analysis for product reliability, and ensures documentation compliance.
9 Days Ago
Juncos, PRI
Biotech • Pharmaceutical
The Sr Associate EH&S will manage Environmental Health & Safety programs, ensure compliance with regulations, interface with regulatory agencies, design training programs, conduct audits, and potentially supervise support staff. Responsibilities include program design, implementation, developing procedures, and assessing long-term EH&S practices.
9 Days Ago
Juncos, PRI
Biotech • Pharmaceutical
The Sr Engineer will lead process optimization and operational troubleshooting in manufacturing environments. Responsibilities include developing engineering policies, supervising junior staff, applying advanced engineering principles, and coordinating major engineering projects within budget and schedule constraints.
17 Days Ago
Conshohocken, PA, USA
Biotech • Pharmaceutical
Seeking experienced Contamination Control Auditors with expertise in Annex 1 projects to conduct gap assessments and report writing. Candidates should possess a Bachelor's degree in Microbiology, over 10 years in pharmaceutical Quality Operations, and strong knowledge of regulatory guidelines and cGMPs. Strong technical writing and communication skills are essential.