Job Description
Thermo Fisher Scientific
Project Director (Gov Contracts)
Thermo Fisher Scientific • Germantown, MD, United States • via Thermo Fisher Scientific Jobs
8 days ago
Full–time
Apply on Thermo Fisher Scientific Jobs
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Apply on LinkedIn
Apply on SimplyHired
Apply on Built In
Apply on Experteer
Apply on Ladders
Apply on Glassdoor
Qualifications
Bachelor of Science degree required
Preferably in Pharmacy
3-5 years of management experience required, preferably Pharmacist staff
+ more items(s)
Benefits
We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits!
The salary range estimated for this position based in Maryland is $130,000.00–$1+4,+00.00
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy
7 more items(s)
Responsibilities
Standard (Mon-Fri)
The Project Director is responsible for the overall operational management of the DMID-CMS government contract, budget management, lab services, bio-repository, and pharmaceutical management
This position requires making decisions vital to lead and conducting repository operations, including receipts, storage, inventory, labeling, encapsulation, and distribution of pharmaceuticals, clinical products, and biologics
15 more items(s)
More job highlights
Job description
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Location/Division Specific Information
Based in Germantown, MD. This position is within the Fisher BioServices business unit of Thermo Fisher Scientific.
Discover Impactful Work:
The Project Director is responsible for the overall operational management of the DMID-CMS government contract, budget management, lab services, bio-repository, and pharmaceutical management. This position requires making decisions vital to lead and conducting repository operations, including receipts, storage, inventory, labeling, encapsulation, and distribution of pharmaceuticals, clinical products, and biologics. This position plans, coordinates, and implements operation policies and procedures that ensure compliance with cGMP and CAP regulations. They craft, coordinate, and implement special projects at the request of the DMID Project Officer.
Work Schedule:
8:00 AM to 5:00 PM hours, additional hours as required.
A Day in the Life:
• Responsible as the primary contact for and collaboration with the Project Officer and DMID personnel, clinical site principal investigators, prime vendors, and manufacturers and for fulfilling all contractual requirements.
• Responsible for all DMID-CMS operations, including coordinating clinical agents' requests, shipments, maintenance of all required records, emergency backup procedures, facility & equipment operation, and validation, as well as all day-to-day operations.
• Lead effort ensuring all SOPs are accurate and current, verification of clinical agent and supply inventory, processing of emergency shipments, supervision and training of DMID-CMS staff.
• Lead effort to maintain reference documents related to DMID protocols and production quality documents.
• Responsible for crafting and maintaining quality documents in compliance with FDA regulations and company policies.
• When required, purchase commercially available drugs from FDA-approved sources.
• Maintain the distribution licenses and correspondence with the states' Boards of Pharmacy.
• Develops and leads contract operational budget, monitors and reviews monthly vouchers, reports, and forecasts changes.
• Ensure timely preparation of monthly progress reports, end-of-option period reports, and physical inventory reports.
• Practice and promote equal employment opportunity
• Must demonstrate and promote our core values, build an environment of respect and inclusion, serve as a Role Model Leader to employees
• Develop and maintain a presentation of the site-specific occupational safety and health training following federal, state, and local regulations.
Keys to Success:
Education
• Bachelor of Science degree required. Preferably in Pharmacy. Advanced degree in Pharmacy highly preferred.
Experience
• 3-5 years of management experience required, preferably Pharmacist staff.
• 3 years of project management experience required.
Certificates and/ or Licenses:
• Registered pharmacist in the state of MD preferred.
• TSA certified highly desireable.
Knowledge, Skills, Abilities
• Demonstrate knowledge of state and federal laws and regulations governing pharmacy services, understanding of import/export regulations, knowledge of procedures for handling and shipping biohazardous agents & dangerous goods, and IATA regulations.
• Excellent analytical, problem-solving, research, written, editing, interpersonal, and verbal communication; proficiency in computer skills and in using Internet tools to acquire technical reports from Government and other Web sites.
• Strong interpersonal project management skills and ability to work with multiple projects. Management experience of personnel and facilities.
• Strong Leadership, organization development, and people management skills
• Knowledge and experience with current Good Manufacturing Practices (cGMP) and CAP accreditation requirements.
• Demonstrated understanding of financial management.
Benefits
We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.
Compensation and Benefits
The salary range estimated for this position based in Maryland is $130,000.00–$1+4,+00.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
• A choice of national medical and dental plans, and a national vision plan, including health incentive programs
• Employee assistance and family support programs, including commuter benefits and tuition reimbursement
• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
• Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
Report this listing
Thermo Fisher Scientific
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LVI Associates
Director of Government Affairs
LVI Associates • Durham, NC, United States • via LVI Associates
15 days ago
Full–time
Apply on LVI Associates
Apply on LVI Associates
Qualifications
5+ years of energy policy and state level legislative and regulatory experience
Established network of state officials in the Southeast
Engaged with lobbyist and trade associations in the region
1 more items(s)
Benefits
Salary: $140,000 - $220,000
30% travel
Family-focused benefits and leave
1 more items(s)
Responsibilities
The position will facilitate the growth of the development team with legislative policies, strategies for increasing product sale, and developing a network of industry professionals and stakeholders
Implementing state legislative and regulatory policy strategies
Networking and maintaining relationships with state officials relevant to the renewable energy industry
2 more items(s)
More job highlights
Job description
Title: Director of Government Affairs
Salary: $140,000 - $220,000
Overview and Company Summary: One of the nation's largest IPPs and a leader in clean energy with a strong track record of solar and battery storage projects developed are seeking a Director of Government Affairs to join their Permitting and Policy department covering North and South Carolina and Southeast region. The position will facilitate the growth of the development team with legislative policies, strategies for increasing product sale, and developing a network of industry professionals and stakeholders.
Responsible For:
• Implementing state legislative and regulatory policy strategies
• Networking and maintaining relationships with state officials relevant to the renewable energy industry
• Working closely with the development team and handling state level policies that may impact their department
• Working with trade associations and lobbyists
Qualifications:
• 5+ years of energy policy and state level legislative and regulatory experience
• Established network of state officials in the Southeast
• Engaged with lobbyist and trade associations in the region
• Experience in project development, specifically utility scale projects
Benefits/perks:
• 30% travel
• Family-focused benefits and leave
• Diverse group of experienced and innovative thinkers
Project Director (Gov Contracts)
Thermo Fisher Scientific • Germantown, MD, United States • via Thermo Fisher Scientific Jobs
8 days ago
Full–time
Apply on Thermo Fisher Scientific Jobs
Apply on ZipRecruiter
Apply on LinkedIn
Apply on SimplyHired
Apply on Built In
Apply on Experteer
Apply on Ladders
Apply on Glassdoor
Qualifications
Bachelor of Science degree required
Preferably in Pharmacy
3-5 years of management experience required, preferably Pharmacist staff
+ more items(s)
Benefits
We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits!
The salary range estimated for this position based in Maryland is $130,000.00–$1+4,+00.00
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy
7 more items(s)
Responsibilities
Standard (Mon-Fri)
The Project Director is responsible for the overall operational management of the DMID-CMS government contract, budget management, lab services, bio-repository, and pharmaceutical management
This position requires making decisions vital to lead and conducting repository operations, including receipts, storage, inventory, labeling, encapsulation, and distribution of pharmaceuticals, clinical products, and biologics
15 more items(s)
More job highlights
Job description
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Location/Division Specific Information
Based in Germantown, MD. This position is within the Fisher BioServices business unit of Thermo Fisher Scientific.
Discover Impactful Work:
The Project Director is responsible for the overall operational management of the DMID-CMS government contract, budget management, lab services, bio-repository, and pharmaceutical management. This position requires making decisions vital to lead and conducting repository operations, including receipts, storage, inventory, labeling, encapsulation, and distribution of pharmaceuticals, clinical products, and biologics. This position plans, coordinates, and implements operation policies and procedures that ensure compliance with cGMP and CAP regulations. They craft, coordinate, and implement special projects at the request of the DMID Project Officer.
Work Schedule:
8:00 AM to 5:00 PM hours, additional hours as required.
A Day in the Life:
• Responsible as the primary contact for and collaboration with the Project Officer and DMID personnel, clinical site principal investigators, prime vendors, and manufacturers and for fulfilling all contractual requirements.
• Responsible for all DMID-CMS operations, including coordinating clinical agents' requests, shipments, maintenance of all required records, emergency backup procedures, facility & equipment operation, and validation, as well as all day-to-day operations.
• Lead effort ensuring all SOPs are accurate and current, verification of clinical agent and supply inventory, processing of emergency shipments, supervision and training of DMID-CMS staff.
• Lead effort to maintain reference documents related to DMID protocols and production quality documents.
• Responsible for crafting and maintaining quality documents in compliance with FDA regulations and company policies.
• When required, purchase commercially available drugs from FDA-approved sources.
• Maintain the distribution licenses and correspondence with the states' Boards of Pharmacy.
• Develops and leads contract operational budget, monitors and reviews monthly vouchers, reports, and forecasts changes.
• Ensure timely preparation of monthly progress reports, end-of-option period reports, and physical inventory reports.
• Practice and promote equal employment opportunity
• Must demonstrate and promote our core values, build an environment of respect and inclusion, serve as a Role Model Leader to employees
• Develop and maintain a presentation of the site-specific occupational safety and health training following federal, state, and local regulations.
Keys to Success:
Education
• Bachelor of Science degree required. Preferably in Pharmacy. Advanced degree in Pharmacy highly preferred.
Experience
• 3-5 years of management experience required, preferably Pharmacist staff.
• 3 years of project management experience required.
Certificates and/ or Licenses:
• Registered pharmacist in the state of MD preferred.
• TSA certified highly desireable.
Knowledge, Skills, Abilities
• Demonstrate knowledge of state and federal laws and regulations governing pharmacy services, understanding of import/export regulations, knowledge of procedures for handling and shipping biohazardous agents & dangerous goods, and IATA regulations.
• Excellent analytical, problem-solving, research, written, editing, interpersonal, and verbal communication; proficiency in computer skills and in using Internet tools to acquire technical reports from Government and other Web sites.
• Strong interpersonal project management skills and ability to work with multiple projects. Management experience of personnel and facilities.
• Strong Leadership, organization development, and people management skills
• Knowledge and experience with current Good Manufacturing Practices (cGMP) and CAP accreditation requirements.
• Demonstrated understanding of financial management.
Benefits
We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.
Compensation and Benefits
The salary range estimated for this position based in Maryland is $130,000.00–$1+4,+00.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
• A choice of national medical and dental plans, and a national vision plan, including health incentive programs
• Employee assistance and family support programs, including commuter benefits and tuition reimbursement
• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
• Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
Report this listing
Thermo Fisher Scientific
Glassdoor
3.6/5
13.4K reviews
AmbitionBox
3.+/5
81+ reviews
Indeed
3.4/5
5.2K reviews
thermofisher.com/us/en/home.html
More jobs at Thermo Fisher Scientific
See web results for Thermo Fisher Scientific
LVI Associates
Director of Government Affairs
LVI Associates • Durham, NC, United States • via LVI Associates
15 days ago
Full–time
Apply on LVI Associates
Apply on LVI Associates
Qualifications
5+ years of energy policy and state level legislative and regulatory experience
Established network of state officials in the Southeast
Engaged with lobbyist and trade associations in the region
1 more items(s)
Benefits
Salary: $140,000 - $220,000
30% travel
Family-focused benefits and leave
1 more items(s)
Responsibilities
The position will facilitate the growth of the development team with legislative policies, strategies for increasing product sale, and developing a network of industry professionals and stakeholders
Implementing state legislative and regulatory policy strategies
Networking and maintaining relationships with state officials relevant to the renewable energy industry
2 more items(s)
More job highlights
Job description
Title: Director of Government Affairs
Salary: $140,000 - $220,000
Overview and Company Summary: One of the nation's largest IPPs and a leader in clean energy with a strong track record of solar and battery storage projects developed are seeking a Director of Government Affairs to join their Permitting and Policy department covering North and South Carolina and Southeast region. The position will facilitate the growth of the development team with legislative policies, strategies for increasing product sale, and developing a network of industry professionals and stakeholders.
Responsible For:
• Implementing state legislative and regulatory policy strategies
• Networking and maintaining relationships with state officials relevant to the renewable energy industry
• Working closely with the development team and handling state level policies that may impact their department
• Working with trade associations and lobbyists
Qualifications:
• 5+ years of energy policy and state level legislative and regulatory experience
• Established network of state officials in the Southeast
• Engaged with lobbyist and trade associations in the region
• Experience in project development, specifically utility scale projects
Benefits/perks:
• 30% travel
• Family-focused benefits and leave
• Diverse group of experienced and innovative thinkers
💡 Quick Summary
Seeking a career-building opportunity? The Director of Government Affairs position is now open for candidates interested in the Government Job Alert sector. This role in Abbeville offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Government Job Alert is a plus.
