PR · On-site
Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include ...
PR · On-site
Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include ...
PR · On-site
Salary: 90,000$ -120,000$ Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries.
Quick apply
PR · On-site
Salary: 90,000$ -120,000$ Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries.
Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include ...
Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include ...
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... The Senior Director of Operational Excellence will lead the strategy, governance, transformation ...
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... The Senior Director of Operational Excellence will lead the strategy, governance, transformation ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Must be fully bilingual (English / Spanish) with excellent oral skills. * Strong knowledge in ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Must be fully bilingual (English / Spanish) with excellent oral skills. * Strong knowledge in ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Must be fully bilingual (English / Spanish) with excellent oral skills. * Strong knowledge in ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Must be fully bilingual (English / Spanish) with excellent oral skills. * Strong knowledge in ...
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
PR · On-site
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Quick apply
Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. At Validation & Engineering Group, people always come first. We believe that when you're ...
Biotech Director information
What are some common challenges faced by Biotech Directors and how are they addressed?
Biotech Directors often encounter challenges such as balancing regulatory compliance with innovation, managing cross-functional teams, and adapting to fast-paced advancements in technology. Addressing these issues requires staying informed on industry regulations, fostering a culture of open communication, and implementing effective project management strategies. Directors typically work closely with scientists, regulatory specialists, and business development teams to align project timelines, budgets, and objectives. Overcoming these challenges is a rewarding aspect of the role and helps drive organizational success in a competitive industry.
What are the key skills and qualifications needed to thrive in the Biotech Director position, and why are they important?
To thrive as a Biotech Director, you need advanced expertise in biotechnology, project management, and leadership, usually demonstrated by a relevant advanced degree and substantial industry experience. Familiarity with laboratory information management systems (LIMS), regulatory compliance protocols (such as FDA or EMA), and certifications like PMP or Six Sigma are highly valued. Excellent communication, problem-solving, and team-building skills help Biotech Directors effectively coordinate multidisciplinary teams and drive innovation. These skills and qualities ensure projects are completed efficiently, regulatory standards are met, and company goals in research and product development are achieved.
What does a Biotech Director do?
A Biotech Director oversees research, development, and operational strategies in a biotechnology company or department. They manage teams, ensure regulatory compliance, and drive innovation to develop new products or therapies. Responsibilities often include budgeting, partnerships, and aligning company goals with scientific advancements. Strong leadership, technical expertise, and industry knowledge are essential for success in this role.
What are the most commonly searched types of Biotech jobs in Puerto Rico? The most popular types of Biotech jobs in Puerto Rico are:
What are popular job titles related to Biotech Director jobs in Puerto Rico? For Biotech Director jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Biotech Director jobs in Puerto Rico look for? The top searched job categories for Biotech Director jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Biotech Director jobs? Cities in Puerto Rico with the most Biotech Director job openings:
Other
Posted 18 days ago
Job description
Previous Pharmaceutical/Biotech experience is mandatory for this role.
MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include Project Management, Process, Automation, Facilities and Equipment CQV.
MMR Consulting has offices in Canada, USA, and Australia.
This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in project management, commissioning and qualification, of equipment, systems and facilities.
This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities. The work will require working out of client's facilities.
The work will require working on-site at client's facilities, which are located in US. Travel is required to US is required.
Responsibilities
Feasibility Assessments
Concept Design, Basic Design, Detailed Design
Procurement
Construction / Installation
Project Controls - Monitoring
Commissioning & Qualification
Qualifications
Salary range: 110,000$ -150,000$ based on experience.
Equal Employment Opportunity and Reasonable Accommodations
MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.
MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include Project Management, Process, Automation, Facilities and Equipment CQV.
MMR Consulting has offices in Canada, USA, and Australia.
This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in project management, commissioning and qualification, of equipment, systems and facilities.
This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities. The work will require working out of client's facilities.
The work will require working on-site at client's facilities, which are located in US. Travel is required to US is required.
Responsibilities
- Provide technical guidance into the assessments, design, project management, commissioning and start-up of equipment and facilities, for upgrades, renovations and expansions of client facilities and processes.
- Prepare business cases, with project purpose, risks, budget, schedule, resource requirements.
- Manage other design firms, equipment vendors, construction firms and internal / external stakeholders as required to execute projects.
- Manage Capital Projects
- Lead or support project execution from feasibility through to project completion/handover, including all project stages such as:
Feasibility Assessments
Concept Design, Basic Design, Detailed Design
Procurement
Construction / Installation
Project Controls - Monitoring
Commissioning & Qualification
- Review and approve technical documentation such as P&IDs, specifications, layouts, manuals, datasheets.
- Integrate safety into the design and execution of all projects (HAZOP reviews, PHSRs, design reviews with EHS representatives).
- Prepare/review automation sequences, as required for Process Automation.
- Engage and coordinate with other other cross-functional departments (Process, automation, building / facilities, procurement, construction management, commissioning, qualification & validation, manufacturing operations, EHS, quality & compliance).
- Facilitate project management tools throughout the execution of projects, such as procurement tracking, vendor management, meeting minutes / action lists, risk register log, schedule updates, project updates.
- Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, provide updates.
- Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).
- Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification & validation phases.
- You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
- Visit construction and installation sites, wear necessary safety PPE.
- Supervise contractors during critical installations of process equipment and associated utilities.
- Other duties as assigned by client, and/or MMR, based on workload and project requirements.
Qualifications
- 12+ years of experience in the biotech industry in project management of various equipment and facilities within the pharmaceutical/biotech industry, with knowledge of requirements for a cGMP operation.
- Previous PM capital projects experience is required.
- Previous Greenfield projects experience is required.
- Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexity.
- Possess mentorship skills, to coach and develop junior and intermediate employees.
- Basic knowledge of AutoCAD.
- Degree, preferably in Mechanical, Chemical, Electrical or other industry related discipline.
- Certification in Project Management would be an asset.
- Travel may be required on occasion. Ability to travel to the US would be an asset.
Salary range: 110,000$ -150,000$ based on experience.
Equal Employment Opportunity and Reasonable Accommodations
MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.
About MMR Consulting
Sourced by ZipRecruiter
Company size
51 - 200 Employees
Headquarters location
Orland Park, IL, US
Year founded
2017