Location: Brighton, MI
Company: Bryllan
and experience you've gained from your education and career, along with willingness to continuously learn in the medical manufacturing industry. If you feel invigorated by the thought of contributing to the creation of life enhancing or lifesaving products, this opportunity could be for you!
Bryllan LLC is a privately owned, rapidly growing Contract Manufacturing Organization (CMO) that has designed a unique sterile filling and containment platform for multi-product filling of cytotoxic, potent, live virus and vaccine, and hormone drug products. We offer a rewarding work environment while maintaining a small company, employee-focused atmosphere. Bryllan differentiates itself from our
competitors by living our values of Quality, Integrity, and Service. The Analytical Chemist conducts responsibilities under the supervision and direction of Analytical Services Management.
The Analytical Chemist is part of the New Product Introduction (NPI) team responsible for onboarding new projects at Bryllan from an analytical perspective. The Analytical Chemist's main responsibility is to support the onboarding of in-process, release, and stability methodologies for chemistry and microbiology backssments. The Analytical Chemist is responsible for development and validation of in-house methods, transferring client methods, and managing third-party outsourced methods that meet all
standards required for c GMP regulations. Various techniques are utilized in the shared Quality Control laboratory including HPLC, GC, and multiple types of spectrophotometry.
As an NPI team member, the Analytical Chemist is responsible for attending weekly client calls. The Analytical Chemist is responsible for collaborating with Process Development, Engineering, Project Management, and Quality Assurance to meet client needs. The Analytical Chemist is a member of the Quality Operations team, responsible for the safe and efficient manufacturing and oversight of drug products. Essential Duties and Responsibilities: Under the supervision of Analytical Services management, conduct guided development, validation, and transfer of methodologies into the Bryllan Quality Control Laboratory.
NPI project delivery; responsible for meeting Bryllan/client project timelines and deliverables. Oversight and coordination of analyses at third-party laboratories. Document laboratory work using laboratory notebooks/worksheets in a detailed and accurate manner that meets c GMP requirements. Investigate and troubleshoot Quality Control methods. Peer review of data, reports, and notebooks to ensure accuracy of raw data and calculations. Perform all work using appropriate safety measures and personal protective equipment.
Assist in training others in laboratory procedures. Participate in laboratory investigations. Performance of analytical assays to test the integrity and identity of raw materials, excipients and finished products, as necessary. Assist with maintaining the laboratory consumables inventory and laboratory housekeeping, as necessary. Specific Position Duties and Responsibilities: Experience with and application of c GMPs, USP/NF, FDA Guidelines and ICH Guidelines Development, troubleshooting, and validation of analytical methods. Installing, qualifying, calibrating, troubleshooting, and maintaining laboratory instruments and equipment Write and execute validation and method transfer protocols, conferring with management and external customers.
Write & review Standard Operating Procedures (SOPs) and other controlled documents. Maintain procedures for accuracy and compliance. Provide immediate, effective response to laboratory errors, deviations and investigations. Behavioral Expectations: Strong work ethic and ability to accomplish tasks without supervision Adhere to and follow all Company Policies and Procedures Excellent interpersonal skills with the ability to cooperate with others in a high-performance setting Basic computer skills (proficient in Microsoft Office applications) Strong mathematical and organizational skills Excellent English communication skills, both written and verbal Must possess honesty, integrity and a commitment to the highest legal and ethical standards Ability to treat every person with courtesy and respect Demonstrate ownership and accountability to production schedule without compromising product quality Knowledge of fundamental c GMP and regulatory principles such as deviations and CAPA Physical Expectations: Frequent lifting, bending, stooping, squatting, pushing, and pulling.
Long periods of sitting and walking. Long periods of sitting, typing, computer entry, or looking at a computer. Work Experience and Education Requirements: Minimum of 2 years' experience in the medical industry, or equivalent relevant experience. Minimum of 2 years' experience using HPLC in a laboratory environment, or equivalent relevant experience. Minimum of 6 months' experience executing supervised method development and validation, or equivalent relevant experience. Four-year degree in Chemistry, Biology, a related Life Science, or equivalent.
Working knowledge of standard software applications such as Chromatography Data Systems, Microsoft Office, and ERP. Working knowledge of Agilent Open Lab CDS or Agilent Chem Station is a plus.
primary care and specialty physicians. Excellent customer service skills and the ability to work in a fast-paced environment are a must. In addition, for 15 consecutive years, residents of Greater Toledo have named us the Consumer Choice Award winner in our market.
In fact, we’re the only hospital in northwest Ohio to receive this honor. REPORTING RELATIONSHIPS/SUPERVISORY RESPONSIBILITIES Phlebotomist reports to department leader with no direct reports. POSITION SUMMARY Performs routine and special blood specimen collection for all age specific patients. ACCOUNTABILITIES – All Essential to the Role Collects products or specimens for basic procedures and may perform point-of-care testing
using proper techniques. Follows strict principles of asepsis and antisepsis. Assists in the care of the patient prior to, during and after specimen collection.
Determines, from like samples, combinations of tests and the associated acceptable minimum volumes. Knowledgeable of pre-analytic variables, which may affect specimen analysis. Familiar with test synonyms and abbreviations, and cross-referencing tests to specimen types. Utilizes laboratory computer information system to include all work aides and shortcuts within the system. Utilizes quality assurance data to enhance the services rendered by the section. Recommends changes in procedures to address quality issues and provide customer/patient
satisfaction. Performs and documents quality control procedures.
Acts as a resource and is a liaison between phlebotomy staff and Laboratory /Point of Care Team. Cross trained in defined core job functions and patient care departments. Routinely perform difficult specimen collections, such as re-draws and misses. Assists in the training of new associates or students. As needed, performs all pre-analytic tasks associated with sample preparation including, but not limited to, centrifugation, decanting, and specimen packaging. Maintains established hospital and departmental policies and procedures, objectives, quality assurance, safety, environmental and infection control.
Complies with requirements of accreditation and regulatory agencies by attending mandatory in-services and continuing laboratory education and participating in continuous quality improvement. Maintains and upgrades personal professional development. Maintains appropriate par levels and organizes supplies and equipment in work areas as assigned. Notifies appropriate associate when re-order levels are reached, and equipment needs to be repaired. Maintains protocols and procedures for excellent patient care and follows guidelines for infection control management. Demonstrates good teamwork.
Willingly accepts adjustments to assignments and adapts willingly to changes in workflow and processes. Provides excellent customer service incorporating Pro Medica’s core values. Performs other duties as directed or assigned. REQUIRED QUALIFICATIONS Education: High School diploma or Equivalent. License/Certification/Experience: A diploma from an accredited phlebotomy training institute OR one year phlebotomy experience. Successful completion of an academic program which included substantial practical clinical phlebotomy experience (i. e. 3+ week clinical student rotation program in a hospital setting).
PREFERRED QUALIFICATIONS: Professional registration preferred [i. e. PBT(ASCP)]1 year experience in a high-volume phlebotomy environment WORKING CONDITIONS Personal Protective Equipment: Employee will follow policy and wear all PPE as recommended. Physical Demands: Must be able to continuously move between hospital departments, and floors while maintaining confidentiality on workstations. Must be able to understand directions and be able to communicate and respond to inquiries between all levels of hospital staffing, patient care and requires effective interpersonal skills.
Must be able to tolerate exposure to disease bearing specimens, blood, and body fluids, odorous chemicals, carcinogens, mutagens, low level radiation, electrical hazards, and flammable liquids. Must be prepared to wear appropriate PPE and follow PPE guidelines. Must be able to differentiate colors. Must be able to input and retrieve information from computer. Must be able to move, push, lift or carry materials or equipment weighing up to 50 lbs. up to 75% of the time. Must be able to stand for long periods of time, potentially 100% of shift. Shifts for this position are 12 hours in length, covering the patient care 24 hours a day, seven days a week, including holidays and weekends.
Personal Protective Equipment Provided by the Hospital. Pro Medica is a mission-based, not-for-profit integrated healthcare organizational headquartered in Toledo, Ohio. For more information, please visit Qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, religion, interaction/gender (including pregnancy), interactionual orientation, gender identity or gender expression, age, physical or mental disability, military or protected veteran status, citizenship, familial or marital status, genetics, or any other legally protected category.
In compliance with the Americans with Disabilities Act Amendment Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a job with Pro Medica, please contact Equal Opportunity Employer/Drug-Free Workplace For more details: jobs-search. org/phlebotomist_blissfield-c435348/phlebotomist-toledo-hospital-full-time-nights-blissfield_i1964618768
areas such as emergency medicine and trauma, heart and vascular, oncology, orthopedics, neurology, women’s services, and children’s services. BUSINESS UNIT Pro Medica Monroe Regional Hospital offers a broad range of inpatient and outpatient services in southern Michigan and Ohio.
A national leader in treatment of heart attack, congestive heart failure, pneumonia and surgical care, Pro Medica Monroe Regional Hospital is also a pacesetter in Michigan for obstetrics, emergency care, intensive care, controlling infections and organ donation. Scope of Position: Shares 24-hour accountability with other members of the leadership team for designated performance outcomes related to a specific
clinical service area. The incumbent is a member of the nursing management team and participates in advancing the goals and objectives for patient care services. Participates in organization-wide initiatives as a member of hospital management.
REQUIRED QUALIFICATIONS Education : Bachelor’s Degree in a clinical field required or actively pursuing. Years of Experience : Minimum two years’ experience in a leadership role or equivalent job duties. License : RN License in the State of Michigan Certification : Current BLS certification PREFERRED QUALIFICATIONS Education : Masters of Science in Nursing or related area of study. ADDITIONAL EXPERIENCE Must have or be actively pursuing Masters
of Science in Nursing or related area of study. If actively pursuing degrees, both bachelor’s and master’s level must be completed within five years.
Flexibility in scheduling hours to meet the 24-hour needs of the service area Must have interpersonal skills to deal calmly and effectively with multiple activities involved in the operation of the unit. Pro Medica is a mission-based, not-for-profit integrated healthcare organization headquartered in Toledo, Ohio. For more information, please visit Qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, religion, interaction/gender (including pregnancy), interactionual orientation, gender identity or gender expression, age, physical or mental disability, military or protected veteran status, citizenship, familial or marital status, genetics, or any other legally protected category.
In compliance with the Americans with Disabilities Act Amendment Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a job with Pro Medica, please contact Equal Opportunity Employer/Drug-Free Workplace For more details: jobs-search. org/sciences_riga-c434893/clinical-nurse-manager-nursing-administration-critical-care-unit-full-time-days-riga_i1964618636
