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Sr Supervisor Jobs in Puerto Rico (NOW HIRING)

Inteldot

Process Development Sr Scientist ID 35535

Juncos, PR · On-site

$89K - $121K/yr

Designs, monitors, or conducts strategies with general guidance from the supervisor. * Provides ... May represent the department on project teams under the supervision of a senior scientific staff ...

BDO

Grant Compliance Senior Associate

San Juan, PR · On-site

The Grant Execution Senior Associate is responsible for supporting the full lifecycle of federally ... No direct supervisory responsibilities Provides task-level guidance to Grant Execution Associates ...

BDO USA

Grant Compliance Senior Associate

San Juan, PR · On-site

The Grant Execution Senior Associate is responsible for supporting the full lifecycle of federally ... supervisory responsibilities • Provides task-level guidance to Grant Execution Associates ...

ATS Automation

Senior Automation Engineer

Guaynabo, PR

$104K - $136K/yr

As a Senior Automation Engineer, you will apply your diverse knowledge of engineering principles ... Report any accidents/incidents to supervisor * Assist in investigating accidents/incidents

Nutanix

Quality Senior Engineer

Arecibo, PR · On-site

$70 - $100/hr

The Senior Quality Engineer works closely with Operations, other cross-functional team members and ... Promote and promulgate all MESH Process and Policies to all the employees under his/her supervisor ...

Eaton Corporation

Quality Senior Engineer

Arecibo, PR · On-site

$75 - $105/hr

The Senior Quality Engineer works closely with Operations, other cross-functional team members and ... Promote and promulgate all MESH Process and Policies to all the employees under his/her supervisor ...

Eaton

Senior Quality Engineer

Arecibo, PR · On-site

$76K - $103K/yr

The Senior Quality Engineer works closely with Operations, other cross-functional team members and ... Promote and promulgate all MESH Process and Policies to all the employees under his/her supervisor ...

Eaton

Quality Senior Engineer

Arecibo, PR · On-site

$76K - $103K/yr

The Senior Quality Engineer works closely with Operations, other cross-functional team members and ... Promote and promulgate all MESH Process and Policies to all the employees under his/her supervisor ...

Assurant, Inc

Sr. Auto Claims Analyst

San Juan, PR

Job Purpose The Senior Auto Claims Analyst is a senior individual contributor responsible for ... supervisory authority. Core Competencies * Analytical Judgment: Applies data, contract language ...

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Sr Supervisor information

What is a Sr Supervisor?

Sr Supervisors, or Senior Supervisors, are experienced professionals who oversee teams or departments within an organization. They are responsible for managing staff, ensuring workflow efficiency, implementing company policies, and often handling more complex or sensitive issues that arise. Sr Supervisors typically report to higher-level management and play a key role in training, mentoring, and evaluating junior staff members. Their leadership helps ensure that organizational goals and standards are consistently met.

How does a Sr Supervisor typically balance hands-on oversight with team development responsibilities?

As a Sr Supervisor, you'll often find yourself balancing direct supervision of daily operations with mentoring and developing your team members. This role requires you to delegate tasks effectively while remaining accessible for guidance and support. You'll regularly lead team meetings, set performance expectations, and provide feedback to foster growth. Maintaining open communication and recognizing individual strengths are key to ensuring both productivity and professional development within your team.

What are the key skills and qualifications needed to thrive as a Sr Supervisor, and why are they important?

To thrive as a Sr Supervisor, you need strong leadership abilities, in-depth knowledge of operational processes, and typically several years of relevant supervisory experience. Familiarity with project management tools, performance tracking systems, and sometimes industry-specific certifications is often required. Exceptional communication, conflict resolution, and decision-making skills help set outstanding Sr Supervisors apart. These competencies are crucial for effectively guiding teams, ensuring productivity, and achieving organizational goals.

What is the difference between Sr Supervisor vs Team Lead?

AspectSr SupervisorTeam Lead
Required CredentialsOften requires several years of supervisory experience, relevant certifications may be preferredTypically requires experience in the specific team or project, certifications are less common
Work EnvironmentOversees multiple teams or departments, involved in strategic planningManages a specific team or project, focuses on daily operations
Employer & Industry UsageCommon in manufacturing, construction, and corporate sectorsWidely used in IT, customer service, and retail industries

While both roles involve leadership, a Sr Supervisor generally oversees multiple teams and handles strategic responsibilities, whereas a Team Lead focuses on guiding a specific team or project on a day-to-day basis. The Sr Supervisor position often requires more experience and broader oversight, making it a higher-level supervisory role.

What are popular job titles related to Sr Supervisor jobs in Puerto Rico?

For Sr Supervisor jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Sr Supervisor jobs in Puerto Rico look for?

The top searched job categories for Sr Supervisor jobs in Puerto Rico are:

Sr Supervisor jobs near you
Infographic showing various Sr Supervisor job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution.

Process Development Sr Scientist ID 35535

Inteldot

Juncos, PR • On-site

$89K - $121K/yr

Full-time

Re-posted 18 days ago

Key responsibilities

  • Design, monitor, or conduct scientific experiments to support project goals.

  • Provide data analysis, interpretation, and assess the impact of data on projects.

  • Develop and implement new protocols to address specific issues.

Job description

Inteldot has over 15 years in the life science industry with allocations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Administrative Shift - 8:00AM - 5:00PM
Description:
To independently conceive, design, implement and advance scientific experiments, which contribute to the successful completion of goals and/or projects. Interprets experimental strategies or leads these activities. Provides input to new processes to generate robust and reliable data. Functions as a lead scientific / technical resource or as a project leader.
Responsibilities:
  • Designs, monitors, or conducts strategies with general guidance from the supervisor.
  • Provides data analysis and interpretation and assesses the impact of the data on the project. Keeps current in technical expertise and areas relevant to their function.
  • Monitors field of expertise, including literature and technology development, and communicates relevant observations.
  • Develop and implement new and novel protocols to address specific issues.
  • May represent the department on project teams under the supervision of a senior scientific staff member.
  • May initiate productive collaborations within and outside of the department or company.
  • Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies.
  • Able to develop solutions to routine technical problems of limited scope.
  • Comprehensive understanding of validation protocol execution requirements. In-depth knowledge of validation processes as applied to new equipment installations.

Job Requirements:
  • Experience supporting sterile drug product manufacturing within the pharmaceutical or biotechnology industry.
  • Validation experience in highly regulated industry.
  • Experience in filling validation and work on technical documentation.
  • Hands-on experience with aseptic filling operations, process characterization, process validation (PPQ), technology transfer, and commercial process support.
  • Experience authoring and executing validation protocols, characterization studies, technical reports, investigations, and change controls.
  • Strong knowledge of GMP requirements, aseptic processing principles, contamination control strategy, and pharmaceutical quality systems.
  • Experience performing statistical analysis using JMP or Minitab and applying data-driven approaches to process optimization.
  • Ability to analyze manufacturing data, identify process trends, and recommend scientifically sound solutions.
  • Experience working in cross-functional teams with Manufacturing, Quality, Engineering, Regulatory, and Technical Services.
  • Strong technical writing, communication, presentation, and project management skills.
  • Ability to independently manage multiple projects in a fast-paced manufacturing environment while supporting commercial readiness and continuous process improvement.
  • Experience with single-use technologies, filling equipment, and sterile manufacturing operations is highly desirable
  • Experience with technical data analysis and scientific documentation

Education:
  • Doctorate (PhD, PharmD, or MD) with relevant postdoctoral experience where applicable; or Master's degree with 3+ years of relevant scientific experience; or Bachelor's degree with 5+ years of relevant scientific experience.
  • Science background as Engineering or microbiology is preferred.

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